Canonical Allele Identifier: CA388034310

Gene: ATP7B

Linked Data

• gnomAD v4: 13-51950053-G-A
• MyVariant Identifiers: chr13:g.52524189G>A (hg19) ; chr13:g.51950053G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51950053G>A , CM000675.2:g.51950053G>A	GRCh38
NC_000013.10:g.52524189G>A , CM000675.1:g.52524189G>A	GRCh37
NC_000013.9:g.51422190G>A	NCBI36
NG_008806.1:g.66442C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*517C>T	ENSP00000489512.2:n.*517C>T
ENST00000673864.2:c.*1428C>T	ENSP00000501045.2:n.*1428C>T
ENST00000674147.2:c.2198C>T	ENSP00000500964.2:p.Thr733Ile
ENST00000242839.10:c.2684C>T MANE Select	ENSP00000242839.5:p.Thr895Ile
ENST00000344297.9:c.2198C>T	ENSP00000342559.5:p.Thr733Ile
ENST00000400366.6:c.2351C>T	ENSP00000383217.3:p.Thr784Ile
ENST00000448424.7:c.2432C>T	ENSP00000416738.3:p.Thr811Ile
ENST00000673772.1:c.2450C>T	ENSP00000501168.1:p.Thr817Ile
ENST00000674147.1:c.1754C>T	ENSP00000500964.1:p.Thr585Ile
ENST00000242839.8:c.2684C>T	ENSP00000242839.4:p.Thr895Ile
ENST00000344297.8:c.2198C>T	ENSP00000342559.5:p.Thr733Ile
ENST00000400366.5:c.2351C>T	ENSP00000383217.3:p.Thr784Ile
ENST00000400370.8:c.1394C>T	ENSP00000383221.3:p.Thr465Ile
ENST00000418097.7:c.2684C>T	ENSP00000393343.2:p.Thr895Ile
ENST00000448424.6:c.2450C>T	ENSP00000416738.2:p.Thr817Ile
ENST00000634296.1:c.645C>T
ENST00000634308.1:c.2450C>T	ENSP00000489234.1:p.Thr817Ile
ENST00000634620.1:n.3482C>T
ENST00000634810.1:n.2029C>T
ENST00000634844.1:c.2540C>T	ENSP00000489398.1:p.Thr847Ile
ENST00000635406.1:n.212-3575C>T
NM_000053.3:c.2684C>T	NP_000044.2:p.Thr895Ile
NM_001005918.2:c.2198C>T	NP_001005918.1:p.Thr733Ile
NM_001243182.1:c.2351C>T	NP_001230111.1:p.Thr784Ile
XM_005266423.2:c.2588C>T	XP_005266480.1:p.Thr863Ile
XM_005266424.3:c.2588C>T	XP_005266481.1:p.Thr863Ile
XM_005266427.2:c.2450C>T	XP_005266484.1:p.Thr817Ile
XM_005266428.1:c.2432C>T	XP_005266485.1:p.Thr811Ile
XM_005266430.3:c.2684C>T	XP_005266487.1:p.Thr895Ile
XM_005266431.2:c.2648C>T	XP_005266488.1:p.Thr883Ile
XM_005266432.2:c.2198C>T	XP_005266489.1:p.Thr733Ile
XM_006719837.2:c.2588C>T	XP_006719900.1:p.Thr863Ile
XM_006719838.1:c.500C>T	XP_006719901.1:p.Thr167Ile
XM_006719839.1:c.500C>T	XP_006719902.1:p.Thr167Ile
XM_011535117.1:c.2588C>T	XP_011533419.1:p.Thr863Ile
XM_011535118.1:c.2684C>T	XP_011533420.1:p.Thr895Ile
XM_011535119.1:c.2684C>T	XP_011533421.1:p.Thr895Ile
XM_011535120.1:c.2270C>T	XP_011533422.1:p.Thr757Ile
XM_011535121.1:c.2684C>T	XP_011533423.1:p.Thr895Ile
XM_011535122.1:c.1352C>T	XP_011533424.1:p.Thr451Ile
XR_941601.1:n.2903C>T
XR_941602.1:n.2903C>T
XR_941603.1:n.2903C>T
XR_941604.1:n.2903C>T
NM_001330578.1:c.2450C>T	NP_001317507.1:p.Thr817Ile
NM_001330579.1:c.2432C>T	NP_001317508.1:p.Thr811Ile
XM_005266424.4:c.2588C>T	XP_005266481.1:p.Thr863Ile
XM_005266430.4:c.2684C>T	XP_005266487.1:p.Thr895Ile
XM_005266431.4:c.2648C>T	XP_005266488.1:p.Thr883Ile
XM_006719837.3:c.2588C>T	XP_006719900.1:p.Thr863Ile
XM_011535117.3:c.2588C>T	XP_011533419.1:p.Thr863Ile
XM_017020627.1:c.2588C>T	XP_016876116.1:p.Thr863Ile
NM_000053.4:c.2684C>T MANE Select	NP_000044.2:p.Thr895Ile
NM_001005918.3:c.2198C>T	NP_001005918.1:p.Thr733Ile
NM_001330579.2:c.2432C>T	NP_001317508.1:p.Thr811Ile
NM_001243182.2:c.2351C>T	NP_001230111.1:p.Thr784Ile
NM_001330578.2:c.2450C>T	NP_001317507.1:p.Thr817Ile