Canonical Allele Identifier: CA2091557285
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51964847_51964848delinsTA , CM000675.2:g.51964847_51964848delinsTA GRCh38
NC_000013.10:g.52538983_52538984delinsTA , CM000675.1:g.52538983_52538984delinsTA GRCh37
NC_000013.9:g.51436984_51436985delinsTA NCBI36
NG_008806.1:g.51647_51648delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000634296.2:c.1869+24_1869+25delinsTA ENSP00000489512.2:n.1869+24_1869+25delins...
ENST00000673864.2:c.*613+24_*613+25delinsTA ENSP00000501045.2:n.*613+24_*613+25delins...
ENST00000674147.2:c.1869+24_1869+25delinsTA ENSP00000500964.2:n.1869+24_1869+25delins...
ENST00000242839.10:c.1869+24_1869+25delinsTA MANE Select ENSP00000242839.5:n.1869+24_1869+25delins...
ENST00000344297.9:c.1869+24_1869+25delinsTA ENSP00000342559.5:n.1869+24_1869+25delins...
ENST00000400366.6:c.1536+24_1536+25delinsTA ENSP00000383217.3:n.1536+24_1536+25delins...
ENST00000448424.7:c.1869+24_1869+25delinsTA ENSP00000416738.3:n.1869+24_1869+25delins...
ENST00000483772.2:n.649_650delinsTA
ENST00000673772.1:c.1869+24_1869+25delinsTA ENSP00000501168.1:n.1869+24_1869+25delins...
ENST00000674147.1:c.1425+24_1425+25delinsTA ENSP00000500964.1:n.1425+24_1425+25delins...
ENST00000242839.8:c.1869+24_1869+25delinsTA ENSP00000242839.4:n.1869+24_1869+25delins...
ENST00000344297.8:c.1869+24_1869+25delinsTA ENSP00000342559.5:n.1869+24_1869+25delins...
ENST00000400366.5:c.1536+24_1536+25delinsTA ENSP00000383217.3:n.1536+24_1536+25delins...
ENST00000400370.8:c.1285+9087_1285+9088delinsTA ENSP00000383221.3:n.1285+9087_1285+9088de...
ENST00000418097.7:c.1869+24_1869+25delinsTA ENSP00000393343.2:n.1869+24_1869+25delins...
ENST00000448424.6:c.1869+24_1869+25delinsTA ENSP00000416738.2:n.1869+24_1869+25delins...
ENST00000482841.6:n.1664+5644_1664+5645delinsTA
ENST00000483772.1:n.649_650delinsTA
ENST00000634296.1:c.5+24_5+25delinsTA
ENST00000634308.1:c.1869+24_1869+25delinsTA ENSP00000489234.1:n.1869+24_1869+25delins...
ENST00000634620.1:n.361+24_361+25delinsTA
ENST00000634844.1:c.1869+24_1869+25delinsTA ENSP00000489398.1:n.1869+24_1869+25delins...
ENST00000635406.1:n.212-18370_212-18369delinsTA
NM_000053.3:c.1869+24_1869+25delinsTA NP_000044.2:n.1869+24_1869+25delinsTA
NM_001005918.2:c.1869+24_1869+25delinsTA NP_001005918.1:n.1869+24_1869+25delinsTA
NM_001243182.1:c.1536+24_1536+25delinsTA NP_001230111.1:n.1536+24_1536+25delinsTA
XM_005266423.2:c.1773+24_1773+25delinsTA XP_005266480.1:n.1773+24_1773+25delinsTA
XM_005266424.3:c.1773+24_1773+25delinsTA XP_005266481.1:n.1773+24_1773+25delinsTA
XM_005266427.2:c.1869+24_1869+25delinsTA XP_005266484.1:n.1869+24_1869+25delinsTA
XM_005266428.1:c.1869+24_1869+25delinsTA XP_005266485.1:n.1869+24_1869+25delinsTA
XM_005266430.3:c.1869+24_1869+25delinsTA XP_005266487.1:n.1869+24_1869+25delinsTA
XM_005266431.2:c.1833+24_1833+25delinsTA XP_005266488.1:n.1833+24_1833+25delinsTA
XM_005266432.2:c.1869+24_1869+25delinsTA XP_005266489.1:n.1869+24_1869+25delinsTA
XM_006719837.2:c.1773+24_1773+25delinsTA XP_006719900.1:n.1773+24_1773+25delinsTA
XM_011535117.1:c.1773+24_1773+25delinsTA XP_011533419.1:n.1773+24_1773+25delinsTA
XM_011535118.1:c.1869+24_1869+25delinsTA XP_011533420.1:n.1869+24_1869+25delinsTA
XM_011535119.1:c.1869+24_1869+25delinsTA XP_011533421.1:n.1869+24_1869+25delinsTA
XM_011535120.1:c.1707+3596_1707+3597delinsTA XP_011533422.1:n.1707+3596_1707+3597delin...
XM_011535121.1:c.1869+24_1869+25delinsTA XP_011533423.1:n.1869+24_1869+25delinsTA
XM_011535122.1:c.537+24_537+25delinsTA XP_011533424.1:n.537+24_537+25delinsTA
XR_941601.1:n.2088+24_2088+25delinsTA
XR_941602.1:n.2088+24_2088+25delinsTA
XR_941603.1:n.2088+24_2088+25delinsTA
XR_941604.1:n.2088+24_2088+25delinsTA
NM_001330578.1:c.1869+24_1869+25delinsTA NP_001317507.1:n.1869+24_1869+25delinsTA
NM_001330579.1:c.1869+24_1869+25delinsTA NP_001317508.1:n.1869+24_1869+25delinsTA
XM_005266424.4:c.1773+24_1773+25delinsTA XP_005266481.1:n.1773+24_1773+25delinsTA
XM_005266430.4:c.1869+24_1869+25delinsTA XP_005266487.1:n.1869+24_1869+25delinsTA
XM_005266431.4:c.1833+24_1833+25delinsTA XP_005266488.1:n.1833+24_1833+25delinsTA
XM_006719837.3:c.1773+24_1773+25delinsTA XP_006719900.1:n.1773+24_1773+25delinsTA
XM_011535117.3:c.1773+24_1773+25delinsTA XP_011533419.1:n.1773+24_1773+25delinsTA
XM_017020627.1:c.1773+24_1773+25delinsTA XP_016876116.1:n.1773+24_1773+25delinsTA
NM_000053.4:c.1869+24_1869+25delinsTA MANE Select NP_000044.2:n.1869+24_1869+25delinsTA
NM_001005918.3:c.1869+24_1869+25delinsTA NP_001005918.1:n.1869+24_1869+25delinsTA
NM_001330579.2:c.1869+24_1869+25delinsTA NP_001317508.1:n.1869+24_1869+25delinsTA
NM_001243182.2:c.1536+24_1536+25delinsTA NP_001230111.1:n.1536+24_1536+25delinsTA
NM_001330578.2:c.1869+24_1869+25delinsTA NP_001317507.1:n.1869+24_1869+25delinsTA