Canonical Allele Identifier: CA388020243

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52509814C>G (hg19) ; chr13:g.51935678C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51935678C>G , CM000675.2:g.51935678C>G	GRCh38
NC_000013.10:g.52509814C>G , CM000675.1:g.52509814C>G	GRCh37
NC_000013.9:g.51407815C>G	NCBI36
NG_008806.1:g.80817G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*1689G>C	ENSP00000489512.2:n.*1689G>C
ENST00000673864.2:c.*2783G>C	ENSP00000501045.2:n.*2783G>C
ENST00000674147.2:c.3418G>C	ENSP00000500964.2:p.Gly1140Arg
ENST00000242839.10:c.4039G>C MANE Select	ENSP00000242839.5:p.Gly1347Arg
ENST00000344297.9:c.3418G>C	ENSP00000342559.5:p.Gly1140Arg
ENST00000400366.6:c.3706G>C	ENSP00000383217.3:p.Gly1236Arg
ENST00000448424.7:c.3787G>C	ENSP00000416738.3:p.Gly1263Arg
ENST00000673696.1:n.1362G>C
ENST00000673772.1:c.3805G>C	ENSP00000501168.1:p.Gly1269Arg
ENST00000673867.1:n.4178G>C
ENST00000673923.1:n.905G>C
ENST00000674147.1:c.2974G>C	ENSP00000500964.1:p.Gly992Arg
ENST00000242839.8:c.4039G>C	ENSP00000242839.4:p.Gly1347Arg
ENST00000344297.8:c.3418G>C	ENSP00000342559.5:p.Gly1140Arg
ENST00000400366.5:c.3706G>C	ENSP00000383217.3:p.Gly1236Arg
ENST00000400370.8:c.2749G>C	ENSP00000383221.3:p.Gly917Arg
ENST00000418097.7:c.3844G>C	ENSP00000393343.2:p.Gly1282Arg
ENST00000448424.6:c.3805G>C	ENSP00000416738.2:p.Gly1269Arg
ENST00000634296.1:c.1817G>C
ENST00000634308.1:c.*1140G>C	ENSP00000489234.1:n.*1140G>C
ENST00000634620.1:n.4783G>C
ENST00000634810.1:n.3384G>C
ENST00000634844.1:c.3895G>C	ENSP00000489398.1:p.Gly1299Arg
NM_000053.3:c.4039G>C	NP_000044.2:p.Gly1347Arg
NM_001005918.2:c.3418G>C	NP_001005918.1:p.Gly1140Arg
NM_001243182.1:c.3706G>C	NP_001230111.1:p.Gly1236Arg
XM_005266423.2:c.3943G>C	XP_005266480.1:p.Gly1315Arg
XM_005266424.3:c.3943G>C	XP_005266481.1:p.Gly1315Arg
XM_005266427.2:c.3805G>C	XP_005266484.1:p.Gly1269Arg
XM_005266428.1:c.3787G>C	XP_005266485.1:p.Gly1263Arg
XM_005266430.3:c.4039G>C	XP_005266487.1:p.Gly1347Arg
XM_005266431.2:c.4003G>C	XP_005266488.1:p.Gly1335Arg
XM_005266432.2:c.3553G>C	XP_005266489.1:p.Gly1185Arg
XM_006719837.2:c.3943G>C	XP_006719900.1:p.Gly1315Arg
XM_006719838.1:c.1855G>C	XP_006719901.1:p.Gly619Arg
XM_006719839.1:c.1672G>C	XP_006719902.1:p.Gly558Arg
XM_011535117.1:c.3943G>C	XP_011533419.1:p.Gly1315Arg
XM_011535118.1:c.3904G>C	XP_011533420.1:p.Gly1302Arg
XM_011535119.1:c.3856G>C	XP_011533421.1:p.Gly1286Arg
XM_011535120.1:c.3625G>C	XP_011533422.1:p.Gly1209Arg
XM_011535121.1:c.3526G>C	XP_011533423.1:p.Gly1176Arg
XM_011535122.1:c.2707G>C	XP_011533424.1:p.Gly903Arg
XR_941601.1:n.4258G>C
XR_941602.1:n.4258G>C
XR_941603.1:n.4258G>C
XR_941604.1:n.4258G>C
NM_001330578.1:c.3805G>C	NP_001317507.1:p.Gly1269Arg
NM_001330579.1:c.3787G>C	NP_001317508.1:p.Gly1263Arg
XM_005266424.4:c.3943G>C	XP_005266481.1:p.Gly1315Arg
XM_005266430.4:c.4039G>C	XP_005266487.1:p.Gly1347Arg
XM_005266431.4:c.4003G>C	XP_005266488.1:p.Gly1335Arg
XM_006719837.3:c.3943G>C	XP_006719900.1:p.Gly1315Arg
XM_011535117.3:c.3943G>C	XP_011533419.1:p.Gly1315Arg
XM_017020627.1:c.3943G>C	XP_016876116.1:p.Gly1315Arg
NM_000053.4:c.4039G>C MANE Select	NP_000044.2:p.Gly1347Arg
NM_001005918.3:c.3418G>C	NP_001005918.1:p.Gly1140Arg
NM_001330579.2:c.3787G>C	NP_001317508.1:p.Gly1263Arg
NM_001243182.2:c.3706G>C	NP_001230111.1:p.Gly1236Arg
NM_001330578.2:c.3805G>C	NP_001317507.1:p.Gly1269Arg