Canonical Allele Identifier: CA483894213

Gene: ATP7B

Linked Data

• gnomAD v4: 13-51941214-G-T
• MyVariant Identifiers: chr13:g.52515350G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941214G>T , CM000675.2:g.51941214G>T	GRCh38
NC_000013.10:g.52515350G>T , CM000675.1:g.52515350G>T	GRCh37
NC_000013.9:g.51413351G>T	NCBI36
NG_008806.1:g.75281C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1073C>A	ENSP00000489512.2:n.*1073C>A
ENST00000673864.2:c.*2167C>A	ENSP00000501045.2:n.*2167C>A
ENST00000674147.2:c.2802C>A	ENSP00000500964.2:p.Pro934=
ENST00000242839.10:c.3423C>A MANE Select	ENSP00000242839.5:p.Pro1141=
ENST00000344297.9:c.2802C>A	ENSP00000342559.5:p.Pro934=
ENST00000400366.6:c.3090C>A	ENSP00000383217.3:p.Pro1030=
ENST00000448424.7:c.3171C>A	ENSP00000416738.3:p.Pro1057=
ENST00000673772.1:c.3189C>A	ENSP00000501168.1:p.Pro1063=
ENST00000673867.1:n.3562C>A
ENST00000674126.1:n.3786C>A
ENST00000674147.1:c.2358C>A	ENSP00000500964.1:p.Pro786=
ENST00000242839.8:c.3423C>A	ENSP00000242839.4:p.Pro1141=
ENST00000344297.8:c.2802C>A	ENSP00000342559.5:p.Pro934=
ENST00000400366.5:c.3090C>A	ENSP00000383217.3:p.Pro1030=
ENST00000400370.8:c.2133C>A	ENSP00000383221.3:p.Pro711=
ENST00000418097.7:c.3228C>A	ENSP00000393343.2:p.Pro1076=
ENST00000448424.6:c.3189C>A	ENSP00000416738.2:p.Pro1063=
ENST00000634296.1:c.1201C>A
ENST00000634308.1:c.*524C>A	ENSP00000489234.1:n.*524C>A
ENST00000634620.1:n.4167C>A
ENST00000634810.1:n.2768C>A
ENST00000634844.1:c.3279C>A	ENSP00000489398.1:p.Pro1093=
NM_000053.3:c.3423C>A	NP_000044.2:p.Pro1141=
NM_001005918.2:c.2802C>A	NP_001005918.1:p.Pro934=
NM_001243182.1:c.3090C>A	NP_001230111.1:p.Pro1030=
XM_005266423.2:c.3327C>A	XP_005266480.1:p.Pro1109=
XM_005266424.3:c.3327C>A	XP_005266481.1:p.Pro1109=
XM_005266427.2:c.3189C>A	XP_005266484.1:p.Pro1063=
XM_005266428.1:c.3171C>A	XP_005266485.1:p.Pro1057=
XM_005266430.3:c.3423C>A	XP_005266487.1:p.Pro1141=
XM_005266431.2:c.3387C>A	XP_005266488.1:p.Pro1129=
XM_005266432.2:c.2937C>A	XP_005266489.1:p.Pro979=
XM_006719837.2:c.3327C>A	XP_006719900.1:p.Pro1109=
XM_006719838.1:c.1239C>A	XP_006719901.1:p.Pro413=
XM_006719839.1:c.1056C>A	XP_006719902.1:p.Pro352=
XM_011535117.1:c.3327C>A	XP_011533419.1:p.Pro1109=
XM_011535118.1:c.3288C>A	XP_011533420.1:p.Pro1096=
XM_011535119.1:c.3240C>A	XP_011533421.1:p.Pro1080=
XM_011535120.1:c.3009C>A	XP_011533422.1:p.Pro1003=
XM_011535121.1:c.2910C>A	XP_011533423.1:p.Pro970=
XM_011535122.1:c.2091C>A	XP_011533424.1:p.Pro697=
XR_941601.1:n.3642C>A
XR_941602.1:n.3642C>A
XR_941603.1:n.3642C>A
XR_941604.1:n.3642C>A
NM_001330578.1:c.3189C>A	NP_001317507.1:p.Pro1063=
NM_001330579.1:c.3171C>A	NP_001317508.1:p.Pro1057=
XM_005266424.4:c.3327C>A	XP_005266481.1:p.Pro1109=
XM_005266430.4:c.3423C>A	XP_005266487.1:p.Pro1141=
XM_005266431.4:c.3387C>A	XP_005266488.1:p.Pro1129=
XM_006719837.3:c.3327C>A	XP_006719900.1:p.Pro1109=
XM_011535117.3:c.3327C>A	XP_011533419.1:p.Pro1109=
XM_017020627.1:c.3327C>A	XP_016876116.1:p.Pro1109=
NM_000053.4:c.3423C>A MANE Select	NP_000044.2:p.Pro1141=
NM_001005918.3:c.2802C>A	NP_001005918.1:p.Pro934=
NM_001330579.2:c.3171C>A	NP_001317508.1:p.Pro1057=
NM_001243182.2:c.3090C>A	NP_001230111.1:p.Pro1030=
NM_001330578.2:c.3189C>A	NP_001317507.1:p.Pro1063=