Canonical Allele Identifier: CA388031761

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52520428C>G (hg19) ; chr13:g.51946292C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51946292C>G , CM000675.2:g.51946292C>G	GRCh38
NC_000013.10:g.52520428C>G , CM000675.1:g.52520428C>G	GRCh37
NC_000013.9:g.51418429C>G	NCBI36
NG_008806.1:g.70203G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*885G>C	ENSP00000489512.2:n.*885G>C
ENST00000673864.2:c.*1796G>C	ENSP00000501045.2:n.*1796G>C
ENST00000674147.2:c.2431G>C	ENSP00000500964.2:p.Ala811Pro
ENST00000242839.10:c.3052G>C MANE Select	ENSP00000242839.5:p.Ala1018Pro
ENST00000344297.9:c.2431G>C	ENSP00000342559.5:p.Ala811Pro
ENST00000400366.6:c.2719G>C	ENSP00000383217.3:p.Ala907Pro
ENST00000448424.7:c.2800G>C	ENSP00000416738.3:p.Ala934Pro
ENST00000673772.1:c.2818G>C	ENSP00000501168.1:p.Ala940Pro
ENST00000673867.1:n.1199G>C
ENST00000674126.1:n.3415G>C
ENST00000674147.1:c.1987G>C	ENSP00000500964.1:p.Ala663Pro
ENST00000242839.8:c.3052G>C	ENSP00000242839.4:p.Ala1018Pro
ENST00000344297.8:c.2431G>C	ENSP00000342559.5:p.Ala811Pro
ENST00000400366.5:c.2719G>C	ENSP00000383217.3:p.Ala907Pro
ENST00000400370.8:c.1762G>C	ENSP00000383221.3:p.Ala588Pro
ENST00000418097.7:c.2866-2001G>C	ENSP00000393343.2:n.2866-2001G>C
ENST00000448424.6:c.2818G>C	ENSP00000416738.2:p.Ala940Pro
ENST00000466629.1:n.272G>C
ENST00000634296.1:c.1013G>C
ENST00000634308.1:c.*153G>C	ENSP00000489234.1:n.*153G>C
ENST00000634620.1:n.3796G>C
ENST00000634810.1:n.2397G>C
ENST00000634844.1:c.2908G>C	ENSP00000489398.1:p.Ala970Pro
ENST00000635406.1:n.398G>C
NM_000053.3:c.3052G>C	NP_000044.2:p.Ala1018Pro
NM_001005918.2:c.2431G>C	NP_001005918.1:p.Ala811Pro
NM_001243182.1:c.2719G>C	NP_001230111.1:p.Ala907Pro
XM_005266423.2:c.2956G>C	XP_005266480.1:p.Ala986Pro
XM_005266424.3:c.2956G>C	XP_005266481.1:p.Ala986Pro
XM_005266427.2:c.2818G>C	XP_005266484.1:p.Ala940Pro
XM_005266428.1:c.2800G>C	XP_005266485.1:p.Ala934Pro
XM_005266430.3:c.3052G>C	XP_005266487.1:p.Ala1018Pro
XM_005266431.2:c.3016G>C	XP_005266488.1:p.Ala1006Pro
XM_005266432.2:c.2566G>C	XP_005266489.1:p.Ala856Pro
XM_006719837.2:c.2956G>C	XP_006719900.1:p.Ala986Pro
XM_006719838.1:c.868G>C	XP_006719901.1:p.Ala290Pro
XM_006719839.1:c.868G>C	XP_006719902.1:p.Ala290Pro
XM_011535117.1:c.2956G>C	XP_011533419.1:p.Ala986Pro
XM_011535118.1:c.2917G>C	XP_011533420.1:p.Ala973Pro
XM_011535119.1:c.3052G>C	XP_011533421.1:p.Ala1018Pro
XM_011535120.1:c.2638G>C	XP_011533422.1:p.Ala880Pro
XM_011535121.1:c.2730+3715G>C	XP_011533423.1:n.2730+3715G>C
XM_011535122.1:c.1720G>C	XP_011533424.1:p.Ala574Pro
XR_941601.1:n.3271G>C
XR_941602.1:n.3271G>C
XR_941603.1:n.3271G>C
XR_941604.1:n.3271G>C
NM_001330578.1:c.2818G>C	NP_001317507.1:p.Ala940Pro
NM_001330579.1:c.2800G>C	NP_001317508.1:p.Ala934Pro
XM_005266424.4:c.2956G>C	XP_005266481.1:p.Ala986Pro
XM_005266430.4:c.3052G>C	XP_005266487.1:p.Ala1018Pro
XM_005266431.4:c.3016G>C	XP_005266488.1:p.Ala1006Pro
XM_006719837.3:c.2956G>C	XP_006719900.1:p.Ala986Pro
XM_011535117.3:c.2956G>C	XP_011533419.1:p.Ala986Pro
XM_017020627.1:c.2956G>C	XP_016876116.1:p.Ala986Pro
NM_000053.4:c.3052G>C MANE Select	NP_000044.2:p.Ala1018Pro
NM_001005918.3:c.2431G>C	NP_001005918.1:p.Ala811Pro
NM_001330579.2:c.2800G>C	NP_001317508.1:p.Ala934Pro
NM_001243182.2:c.2719G>C	NP_001230111.1:p.Ala907Pro
NM_001330578.2:c.2818G>C	NP_001317507.1:p.Ala940Pro