Canonical Allele Identifier: CA2623118852

Gene: ATP7B

Linked Data

• gnomAD v4: 13-51970559-T-TAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51970563_51970565dup , CM000675.2:g.51970563_51970565dup	GRCh38
NC_000013.10:g.52544699_52544701dup , CM000675.1:g.52544699_52544701dup	GRCh37
NC_000013.9:g.51442700_51442702dup	NCBI36
NG_008806.1:g.45933_45935dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.1473_1475dup	ENSP00000489512.2:p.Phe491_Leu492insPhe
ENST00000673864.2:c.*217_*219dup	ENSP00000501045.2:n.*217_*219dup
ENST00000674147.2:c.1473_1475dup	ENSP00000500964.2:p.Phe491_Leu492insPhe
ENST00000242839.10:c.1473_1475dup MANE Select	ENSP00000242839.5:p.Phe491_Leu492insPhe
ENST00000344297.9:c.1473_1475dup	ENSP00000342559.5:p.Phe491_Leu492insPhe
ENST00000400366.6:c.1140_1142dup	ENSP00000383217.3:p.Phe380_Leu381insPhe
ENST00000448424.7:c.1473_1475dup	ENSP00000416738.3:p.Phe491_Leu492insPhe
ENST00000483772.2:n.229_231dup
ENST00000673772.1:c.1473_1475dup	ENSP00000501168.1:p.Phe491_Leu492insPhe
ENST00000673789.1:n.429_431dup
ENST00000673864.1:c.667_669dup	ENSP00000501045.1:n.667_669dup
ENST00000674078.1:n.1574_1576dup
ENST00000674147.1:c.1029_1031dup	ENSP00000500964.1:p.Phe343_Leu344insPhe
ENST00000242839.8:c.1473_1475dup	ENSP00000242839.4:p.Phe491_Leu492insPhe
ENST00000344297.8:c.1473_1475dup	ENSP00000342559.5:p.Phe491_Leu492insPhe
ENST00000400366.5:c.1140_1142dup	ENSP00000383217.3:p.Phe380_Leu381insPhe
ENST00000400370.8:c.1285+3373_1285+3375dup	ENSP00000383221.3:n.1285+3373_1285+3375du...
ENST00000418097.7:c.1473_1475dup	ENSP00000393343.2:p.Phe491_Leu492insPhe
ENST00000448424.6:c.1473_1475dup	ENSP00000416738.2:p.Phe491_Leu492insPhe
ENST00000482841.6:n.1594_1596dup
ENST00000483772.1:n.229_231dup
ENST00000634308.1:c.1473_1475dup	ENSP00000489234.1:p.Phe491_Leu492insPhe
ENST00000634844.1:c.1473_1475dup	ENSP00000489398.1:p.Phe491_Leu492insPhe
ENST00000635406.1:n.212-24084_212-24082dup
NM_000053.3:c.1473_1475dup	NP_000044.2:p.Phe491_Leu492insPhe
NM_001005918.2:c.1473_1475dup	NP_001005918.1:p.Phe491_Leu492insPhe
NM_001243182.1:c.1140_1142dup	NP_001230111.1:p.Phe380_Leu381insPhe
XM_005266423.2:c.1377_1379dup	XP_005266480.1:p.Phe459_Leu460insPhe
XM_005266424.3:c.1377_1379dup	XP_005266481.1:p.Phe459_Leu460insPhe
XM_005266427.2:c.1473_1475dup	XP_005266484.1:p.Phe491_Leu492insPhe
XM_005266428.1:c.1473_1475dup	XP_005266485.1:p.Phe491_Leu492insPhe
XM_005266430.3:c.1473_1475dup	XP_005266487.1:p.Phe491_Leu492insPhe
XM_005266431.2:c.1437_1439dup	XP_005266488.1:p.Phe479_Leu480insPhe
XM_005266432.2:c.1473_1475dup	XP_005266489.1:p.Phe491_Leu492insPhe
XM_006719837.2:c.1377_1379dup	XP_006719900.1:p.Phe459_Leu460insPhe
XM_011535117.1:c.1377_1379dup	XP_011533419.1:p.Phe459_Leu460insPhe
XM_011535118.1:c.1473_1475dup	XP_011533420.1:p.Phe491_Leu492insPhe
XM_011535119.1:c.1473_1475dup	XP_011533421.1:p.Phe491_Leu492insPhe
XM_011535120.1:c.1473_1475dup	XP_011533422.1:p.Phe491_Leu492insPhe
XM_011535121.1:c.1473_1475dup	XP_011533423.1:p.Phe491_Leu492insPhe
XM_011535122.1:c.141_143dup	XP_011533424.1:p.Phe47_Leu48insPhe
XR_941601.1:n.1692_1694dup
XR_941602.1:n.1692_1694dup
XR_941603.1:n.1692_1694dup
XR_941604.1:n.1692_1694dup
NM_001330578.1:c.1473_1475dup	NP_001317507.1:p.Phe491_Leu492insPhe
NM_001330579.1:c.1473_1475dup	NP_001317508.1:p.Phe491_Leu492insPhe
XM_005266424.4:c.1377_1379dup	XP_005266481.1:p.Phe459_Leu460insPhe
XM_005266430.4:c.1473_1475dup	XP_005266487.1:p.Phe491_Leu492insPhe
XM_005266431.4:c.1437_1439dup	XP_005266488.1:p.Phe479_Leu480insPhe
XM_006719837.3:c.1377_1379dup	XP_006719900.1:p.Phe459_Leu460insPhe
XM_011535117.3:c.1377_1379dup	XP_011533419.1:p.Phe459_Leu460insPhe
XM_017020627.1:c.1377_1379dup	XP_016876116.1:p.Phe459_Leu460insPhe
NM_000053.4:c.1473_1475dup MANE Select	NP_000044.2:p.Phe491_Leu492insPhe
NM_001005918.3:c.1473_1475dup	NP_001005918.1:p.Phe491_Leu492insPhe
NM_001330579.2:c.1473_1475dup	NP_001317508.1:p.Phe491_Leu492insPhe
NM_001243182.2:c.1140_1142dup	NP_001230111.1:p.Phe380_Leu381insPhe
NM_001330578.2:c.1473_1475dup	NP_001317507.1:p.Phe491_Leu492insPhe