Canonical Allele Identifier: CA388031711

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 2696251
• ClinVar RCV Id: RCV003502841
• MyVariant Identifiers: chr13:g.52520422T>A (hg19) ; chr13:g.51946286T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51946286T>A , CM000675.2:g.51946286T>A	GRCh38
NC_000013.10:g.52520422T>A , CM000675.1:g.52520422T>A	GRCh37
NC_000013.9:g.51418423T>A	NCBI36
NG_008806.1:g.70209A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*891A>T	ENSP00000489512.2:n.*891A>T
ENST00000673864.2:c.*1802A>T	ENSP00000501045.2:n.*1802A>T
ENST00000674147.2:c.2437A>T	ENSP00000500964.2:p.Lys813Ter
ENST00000242839.10:c.3058A>T MANE Select	ENSP00000242839.5:p.Lys1020Ter
ENST00000344297.9:c.2437A>T	ENSP00000342559.5:p.Lys813Ter
ENST00000400366.6:c.2725A>T	ENSP00000383217.3:p.Lys909Ter
ENST00000448424.7:c.2806A>T	ENSP00000416738.3:p.Lys936Ter
ENST00000673772.1:c.2824A>T	ENSP00000501168.1:p.Lys942Ter
ENST00000673867.1:n.1205A>T
ENST00000674126.1:n.3421A>T
ENST00000674147.1:c.1993A>T	ENSP00000500964.1:p.Lys665Ter
ENST00000242839.8:c.3058A>T	ENSP00000242839.4:p.Lys1020Ter
ENST00000344297.8:c.2437A>T	ENSP00000342559.5:p.Lys813Ter
ENST00000400366.5:c.2725A>T	ENSP00000383217.3:p.Lys909Ter
ENST00000400370.8:c.1768A>T	ENSP00000383221.3:p.Lys590Ter
ENST00000418097.7:c.2866-1995A>T	ENSP00000393343.2:n.2866-1995A>T
ENST00000448424.6:c.2824A>T	ENSP00000416738.2:p.Lys942Ter
ENST00000466629.1:n.278A>T
ENST00000634296.1:c.1019A>T
ENST00000634308.1:c.*159A>T	ENSP00000489234.1:n.*159A>T
ENST00000634620.1:n.3802A>T
ENST00000634810.1:n.2403A>T
ENST00000634844.1:c.2914A>T	ENSP00000489398.1:p.Lys972Ter
ENST00000635406.1:n.404A>T
NM_000053.3:c.3058A>T	NP_000044.2:p.Lys1020Ter
NM_001005918.2:c.2437A>T	NP_001005918.1:p.Lys813Ter
NM_001243182.1:c.2725A>T	NP_001230111.1:p.Lys909Ter
XM_005266423.2:c.2962A>T	XP_005266480.1:p.Lys988Ter
XM_005266424.3:c.2962A>T	XP_005266481.1:p.Lys988Ter
XM_005266427.2:c.2824A>T	XP_005266484.1:p.Lys942Ter
XM_005266428.1:c.2806A>T	XP_005266485.1:p.Lys936Ter
XM_005266430.3:c.3058A>T	XP_005266487.1:p.Lys1020Ter
XM_005266431.2:c.3022A>T	XP_005266488.1:p.Lys1008Ter
XM_005266432.2:c.2572A>T	XP_005266489.1:p.Lys858Ter
XM_006719837.2:c.2962A>T	XP_006719900.1:p.Lys988Ter
XM_006719838.1:c.874A>T	XP_006719901.1:p.Lys292Ter
XM_006719839.1:c.874A>T	XP_006719902.1:p.Lys292Ter
XM_011535117.1:c.2962A>T	XP_011533419.1:p.Lys988Ter
XM_011535118.1:c.2923A>T	XP_011533420.1:p.Lys975Ter
XM_011535119.1:c.3058A>T	XP_011533421.1:p.Lys1020Ter
XM_011535120.1:c.2644A>T	XP_011533422.1:p.Lys882Ter
XM_011535121.1:c.2730+3721A>T	XP_011533423.1:n.2730+3721A>T
XM_011535122.1:c.1726A>T	XP_011533424.1:p.Lys576Ter
XR_941601.1:n.3277A>T
XR_941602.1:n.3277A>T
XR_941603.1:n.3277A>T
XR_941604.1:n.3277A>T
NM_001330578.1:c.2824A>T	NP_001317507.1:p.Lys942Ter
NM_001330579.1:c.2806A>T	NP_001317508.1:p.Lys936Ter
XM_005266424.4:c.2962A>T	XP_005266481.1:p.Lys988Ter
XM_005266430.4:c.3058A>T	XP_005266487.1:p.Lys1020Ter
XM_005266431.4:c.3022A>T	XP_005266488.1:p.Lys1008Ter
XM_006719837.3:c.2962A>T	XP_006719900.1:p.Lys988Ter
XM_011535117.3:c.2962A>T	XP_011533419.1:p.Lys988Ter
XM_017020627.1:c.2962A>T	XP_016876116.1:p.Lys988Ter
NM_000053.4:c.3058A>T MANE Select	NP_000044.2:p.Lys1020Ter
NM_001005918.3:c.2437A>T	NP_001005918.1:p.Lys813Ter
NM_001330579.2:c.2806A>T	NP_001317508.1:p.Lys936Ter
NM_001243182.2:c.2725A>T	NP_001230111.1:p.Lys909Ter
NM_001330578.2:c.2824A>T	NP_001317507.1:p.Lys942Ter