Canonical Allele Identifier: CA2499222499
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1162212
ClinVar RCV Id: RCV001506986
dbSNP Id: rs2139883798

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51968437_51968449del , CM000675.2:g.51968437_51968449del GRCh38
NC_000013.10:g.52542573_52542585del , CM000675.1:g.52542573_52542585del GRCh37
NC_000013.9:g.51440574_51440586del NCBI36
NG_008806.1:g.48049_48061del

Transcript Alleles

HGVS Amino-acid change
ENST00000634296.2:c.1705_1707+10del
ENST00000673864.2:c.*449_*451+10del
ENST00000674147.2:c.1705_1707+10del
ENST00000242839.10:c.1705_1707+10del
ENST00000344297.9:c.1705_1707+10del
ENST00000400366.6:c.1372_1374+10del
ENST00000448424.7:c.1705_1707+10del
ENST00000483772.2:n.461_463+10del
ENST00000673772.1:c.1705_1707+10del
ENST00000673864.1:c.899_901+10del
ENST00000674147.1:c.1261_1263+10del
ENST00000242839.8:c.1705_1707+10del
ENST00000344297.8:c.1705_1707+10del
ENST00000400366.5:c.1372_1374+10del
ENST00000400370.8:c.1285+5489_1285+5501del ENSP00000383221.3:n.1285+5489_1285+5501del
ENST00000418097.7:c.1705_1707+10del
ENST00000448424.6:c.1705_1707+10del
ENST00000482841.6:n.1664+2046_1664+2058del
ENST00000483772.1:n.461_463+10del
ENST00000634308.1:c.1705_1707+10del
ENST00000634620.1:n.197_199+10del
ENST00000634844.1:c.1705_1707+10del
ENST00000635406.1:n.212-21968_212-21956del
NM_000053.3:c.1705_1707+10del
NM_001005918.2:c.1705_1707+10del
NM_001243182.1:c.1372_1374+10del
XM_005266423.2:c.1609_1611+10del
XM_005266424.3:c.1609_1611+10del
XM_005266427.2:c.1705_1707+10del
XM_005266428.1:c.1705_1707+10del
XM_005266430.3:c.1705_1707+10del
XM_005266431.2:c.1669_1671+10del
XM_005266432.2:c.1705_1707+10del
XM_006719837.2:c.1609_1611+10del
XM_011535117.1:c.1609_1611+10del
XM_011535118.1:c.1705_1707+10del
XM_011535119.1:c.1705_1707+10del
XM_011535120.1:c.1705_1707+10del
XM_011535121.1:c.1705_1707+10del
XM_011535122.1:c.373_375+10del
XR_941601.1:n.1924_1926+10del
XR_941602.1:n.1924_1926+10del
XR_941603.1:n.1924_1926+10del
XR_941604.1:n.1924_1926+10del
NM_001330578.1:c.1705_1707+10del
NM_001330579.1:c.1705_1707+10del
XM_005266424.4:c.1609_1611+10del
XM_005266430.4:c.1705_1707+10del
XM_005266431.4:c.1669_1671+10del
XM_006719837.3:c.1609_1611+10del
XM_011535117.3:c.1609_1611+10del
XM_017020627.1:c.1609_1611+10del
NM_000053.4:c.1705_1707+10del
NM_001005918.3:c.1705_1707+10del
NM_001330579.2:c.1705_1707+10del
NM_001243182.2:c.1372_1374+10del
NM_001330578.2:c.1705_1707+10del