Canonical Allele Identifier: CA388034446

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52524208G>A (hg19) ; chr13:g.51950072G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51950072G>A , CM000675.2:g.51950072G>A	GRCh38
NC_000013.10:g.52524208G>A , CM000675.1:g.52524208G>A	GRCh37
NC_000013.9:g.51422209G>A	NCBI36
NG_008806.1:g.66423C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*498C>T	ENSP00000489512.2:n.*498C>T
ENST00000673864.2:c.*1409C>T	ENSP00000501045.2:n.*1409C>T
ENST00000674147.2:c.2179C>T	ENSP00000500964.2:p.His727Tyr
ENST00000242839.10:c.2665C>T MANE Select	ENSP00000242839.5:p.His889Tyr
ENST00000344297.9:c.2179C>T	ENSP00000342559.5:p.His727Tyr
ENST00000400366.6:c.2332C>T	ENSP00000383217.3:p.His778Tyr
ENST00000448424.7:c.2413C>T	ENSP00000416738.3:p.His805Tyr
ENST00000673772.1:c.2431C>T	ENSP00000501168.1:p.His811Tyr
ENST00000674147.1:c.1735C>T	ENSP00000500964.1:p.His579Tyr
ENST00000242839.8:c.2665C>T	ENSP00000242839.4:p.His889Tyr
ENST00000344297.8:c.2179C>T	ENSP00000342559.5:p.His727Tyr
ENST00000400366.5:c.2332C>T	ENSP00000383217.3:p.His778Tyr
ENST00000400370.8:c.1375C>T	ENSP00000383221.3:p.His459Tyr
ENST00000418097.7:c.2665C>T	ENSP00000393343.2:p.His889Tyr
ENST00000448424.6:c.2431C>T	ENSP00000416738.2:p.His811Tyr
ENST00000634296.1:c.626C>T
ENST00000634308.1:c.2431C>T	ENSP00000489234.1:p.His811Tyr
ENST00000634620.1:n.3463C>T
ENST00000634810.1:n.2010C>T
ENST00000634844.1:c.2521C>T	ENSP00000489398.1:p.His841Tyr
ENST00000635406.1:n.212-3594C>T
NM_000053.3:c.2665C>T	NP_000044.2:p.His889Tyr
NM_001005918.2:c.2179C>T	NP_001005918.1:p.His727Tyr
NM_001243182.1:c.2332C>T	NP_001230111.1:p.His778Tyr
XM_005266423.2:c.2569C>T	XP_005266480.1:p.His857Tyr
XM_005266424.3:c.2569C>T	XP_005266481.1:p.His857Tyr
XM_005266427.2:c.2431C>T	XP_005266484.1:p.His811Tyr
XM_005266428.1:c.2413C>T	XP_005266485.1:p.His805Tyr
XM_005266430.3:c.2665C>T	XP_005266487.1:p.His889Tyr
XM_005266431.2:c.2629C>T	XP_005266488.1:p.His877Tyr
XM_005266432.2:c.2179C>T	XP_005266489.1:p.His727Tyr
XM_006719837.2:c.2569C>T	XP_006719900.1:p.His857Tyr
XM_006719838.1:c.481C>T	XP_006719901.1:p.His161Tyr
XM_006719839.1:c.481C>T	XP_006719902.1:p.His161Tyr
XM_011535117.1:c.2569C>T	XP_011533419.1:p.His857Tyr
XM_011535118.1:c.2665C>T	XP_011533420.1:p.His889Tyr
XM_011535119.1:c.2665C>T	XP_011533421.1:p.His889Tyr
XM_011535120.1:c.2251C>T	XP_011533422.1:p.His751Tyr
XM_011535121.1:c.2665C>T	XP_011533423.1:p.His889Tyr
XM_011535122.1:c.1333C>T	XP_011533424.1:p.His445Tyr
XR_941601.1:n.2884C>T
XR_941602.1:n.2884C>T
XR_941603.1:n.2884C>T
XR_941604.1:n.2884C>T
NM_001330578.1:c.2431C>T	NP_001317507.1:p.His811Tyr
NM_001330579.1:c.2413C>T	NP_001317508.1:p.His805Tyr
XM_005266424.4:c.2569C>T	XP_005266481.1:p.His857Tyr
XM_005266430.4:c.2665C>T	XP_005266487.1:p.His889Tyr
XM_005266431.4:c.2629C>T	XP_005266488.1:p.His877Tyr
XM_006719837.3:c.2569C>T	XP_006719900.1:p.His857Tyr
XM_011535117.3:c.2569C>T	XP_011533419.1:p.His857Tyr
XM_017020627.1:c.2569C>T	XP_016876116.1:p.His857Tyr
NM_000053.4:c.2665C>T MANE Select	NP_000044.2:p.His889Tyr
NM_001005918.3:c.2179C>T	NP_001005918.1:p.His727Tyr
NM_001330579.2:c.2413C>T	NP_001317508.1:p.His805Tyr
NM_001243182.2:c.2332C>T	NP_001230111.1:p.His778Tyr
NM_001330578.2:c.2431C>T	NP_001317507.1:p.His811Tyr