Canonical Allele Identifier: CA2623116464

Gene: ATP7B

Linked Data

• gnomAD v4: 13-51944266-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944267del , CM000675.2:g.51944267del	GRCh38
NC_000013.10:g.52518403del , CM000675.1:g.52518403del	GRCh37
NC_000013.9:g.51416404del	NCBI36
NG_008806.1:g.72228del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*894-1713del	ENSP00000489512.2:n.*894-1713del
ENST00000673864.2:c.*1829del	ENSP00000501045.2:n.*1829del
ENST00000674147.2:c.2464del	ENSP00000500964.2:p.Thr822LeufsTer?
ENST00000242839.10:c.3085del MANE Select	ENSP00000242839.5:p.Thr1029LeufsTer?
ENST00000344297.9:c.2464del	ENSP00000342559.5:p.Thr822LeufsTer?
ENST00000400366.6:c.2752del	ENSP00000383217.3:p.Thr918LeufsTer?
ENST00000448424.7:c.2833del	ENSP00000416738.3:p.Thr945LeufsTer?
ENST00000673772.1:c.2851del	ENSP00000501168.1:p.Thr951LeufsTer?
ENST00000673867.1:n.3224del
ENST00000674126.1:n.3448del
ENST00000674147.1:c.2020del	ENSP00000500964.1:p.Thr674LeufsTer?
ENST00000242839.8:c.3085del	ENSP00000242839.4:p.Thr1029LeufsTer?
ENST00000344297.8:c.2464del	ENSP00000342559.5:p.Thr822LeufsTer?
ENST00000400366.5:c.2752del	ENSP00000383217.3:p.Thr918LeufsTer?
ENST00000400370.8:c.1795del	ENSP00000383221.3:p.Thr599LeufsTer?
ENST00000418097.7:c.2890del	ENSP00000393343.2:p.Thr964LeufsTer?
ENST00000448424.6:c.2851del	ENSP00000416738.2:p.Thr951LeufsTer?
ENST00000466629.1:n.305del
ENST00000634296.1:c.1022-1713del
ENST00000634308.1:c.*186del	ENSP00000489234.1:n.*186del
ENST00000634620.1:n.3829del
ENST00000634810.1:n.2430del
ENST00000634844.1:c.2941del	ENSP00000489398.1:p.Thr981LeufsTer?
ENST00000635406.1:n.431del
NM_000053.3:c.3085del	NP_000044.2:p.Thr1029LeufsTer?
NM_001005918.2:c.2464del	NP_001005918.1:p.Thr822LeufsTer?
NM_001243182.1:c.2752del	NP_001230111.1:p.Thr918LeufsTer?
XM_005266423.2:c.2989del	XP_005266480.1:p.Thr997LeufsTer?
XM_005266424.3:c.2989del	XP_005266481.1:p.Thr997LeufsTer?
XM_005266427.2:c.2851del	XP_005266484.1:p.Thr951LeufsTer?
XM_005266428.1:c.2833del	XP_005266485.1:p.Thr945LeufsTer?
XM_005266430.3:c.3085del	XP_005266487.1:p.Thr1029LeufsTer?
XM_005266431.2:c.3049del	XP_005266488.1:p.Thr1017LeufsTer?
XM_005266432.2:c.2599del	XP_005266489.1:p.Thr867LeufsTer?
XM_006719837.2:c.2989del	XP_006719900.1:p.Thr997LeufsTer?
XM_006719838.1:c.901del	XP_006719901.1:p.Thr301LeufsTer?
XM_006719839.1:c.877-1713del	XP_006719902.1:n.877-1713del
XM_011535117.1:c.2989del	XP_011533419.1:p.Thr997LeufsTer?
XM_011535118.1:c.2950del	XP_011533420.1:p.Thr984LeufsTer?
XM_011535119.1:c.3061-1713del	XP_011533421.1:n.3061-1713del
XM_011535120.1:c.2671del	XP_011533422.1:p.Thr891LeufsTer?
XM_011535121.1:c.2731-1713del	XP_011533423.1:n.2731-1713del
XM_011535122.1:c.1753del	XP_011533424.1:p.Thr585LeufsTer?
XR_941601.1:n.3304del
XR_941602.1:n.3304del
XR_941603.1:n.3304del
XR_941604.1:n.3304del
NM_001330578.1:c.2851del	NP_001317507.1:p.Thr951LeufsTer?
NM_001330579.1:c.2833del	NP_001317508.1:p.Thr945LeufsTer?
XM_005266424.4:c.2989del	XP_005266481.1:p.Thr997LeufsTer?
XM_005266430.4:c.3085del	XP_005266487.1:p.Thr1029LeufsTer?
XM_005266431.4:c.3049del	XP_005266488.1:p.Thr1017LeufsTer?
XM_006719837.3:c.2989del	XP_006719900.1:p.Thr997LeufsTer?
XM_011535117.3:c.2989del	XP_011533419.1:p.Thr997LeufsTer?
XM_017020627.1:c.2989del	XP_016876116.1:p.Thr997LeufsTer?
NM_000053.4:c.3085del MANE Select	NP_000044.2:p.Thr1029LeufsTer?
NM_001005918.3:c.2464del	NP_001005918.1:p.Thr822LeufsTer?
NM_001330579.2:c.2833del	NP_001317508.1:p.Thr945LeufsTer?
NM_001243182.2:c.2752del	NP_001230111.1:p.Thr918LeufsTer?
NM_001330578.2:c.2851del	NP_001317507.1:p.Thr951LeufsTer?