Canonical Allele Identifier: CA388034432

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 2505172
• ClinVar RCV Id: RCV003233350
• MyVariant Identifiers: chr13:g.52524205C>A (hg19) ; chr13:g.51950069C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51950069C>A , CM000675.2:g.51950069C>A	GRCh38
NC_000013.10:g.52524205C>A , CM000675.1:g.52524205C>A	GRCh37
NC_000013.9:g.51422206C>A	NCBI36
NG_008806.1:g.66426G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*501G>T	ENSP00000489512.2:n.*501G>T
ENST00000673864.2:c.*1412G>T	ENSP00000501045.2:n.*1412G>T
ENST00000674147.2:c.2182G>T	ENSP00000500964.2:p.Val728Leu
ENST00000242839.10:c.2668G>T MANE Select	ENSP00000242839.5:p.Val890Leu
ENST00000344297.9:c.2182G>T	ENSP00000342559.5:p.Val728Leu
ENST00000400366.6:c.2335G>T	ENSP00000383217.3:p.Val779Leu
ENST00000448424.7:c.2416G>T	ENSP00000416738.3:p.Val806Leu
ENST00000673772.1:c.2434G>T	ENSP00000501168.1:p.Val812Leu
ENST00000674147.1:c.1738G>T	ENSP00000500964.1:p.Val580Leu
ENST00000242839.8:c.2668G>T	ENSP00000242839.4:p.Val890Leu
ENST00000344297.8:c.2182G>T	ENSP00000342559.5:p.Val728Leu
ENST00000400366.5:c.2335G>T	ENSP00000383217.3:p.Val779Leu
ENST00000400370.8:c.1378G>T	ENSP00000383221.3:p.Val460Leu
ENST00000418097.7:c.2668G>T	ENSP00000393343.2:p.Val890Leu
ENST00000448424.6:c.2434G>T	ENSP00000416738.2:p.Val812Leu
ENST00000634296.1:c.629G>T
ENST00000634308.1:c.2434G>T	ENSP00000489234.1:p.Val812Leu
ENST00000634620.1:n.3466G>T
ENST00000634810.1:n.2013G>T
ENST00000634844.1:c.2524G>T	ENSP00000489398.1:p.Val842Leu
ENST00000635406.1:n.212-3591G>T
NM_000053.3:c.2668G>T	NP_000044.2:p.Val890Leu
NM_001005918.2:c.2182G>T	NP_001005918.1:p.Val728Leu
NM_001243182.1:c.2335G>T	NP_001230111.1:p.Val779Leu
XM_005266423.2:c.2572G>T	XP_005266480.1:p.Val858Leu
XM_005266424.3:c.2572G>T	XP_005266481.1:p.Val858Leu
XM_005266427.2:c.2434G>T	XP_005266484.1:p.Val812Leu
XM_005266428.1:c.2416G>T	XP_005266485.1:p.Val806Leu
XM_005266430.3:c.2668G>T	XP_005266487.1:p.Val890Leu
XM_005266431.2:c.2632G>T	XP_005266488.1:p.Val878Leu
XM_005266432.2:c.2182G>T	XP_005266489.1:p.Val728Leu
XM_006719837.2:c.2572G>T	XP_006719900.1:p.Val858Leu
XM_006719838.1:c.484G>T	XP_006719901.1:p.Val162Leu
XM_006719839.1:c.484G>T	XP_006719902.1:p.Val162Leu
XM_011535117.1:c.2572G>T	XP_011533419.1:p.Val858Leu
XM_011535118.1:c.2668G>T	XP_011533420.1:p.Val890Leu
XM_011535119.1:c.2668G>T	XP_011533421.1:p.Val890Leu
XM_011535120.1:c.2254G>T	XP_011533422.1:p.Val752Leu
XM_011535121.1:c.2668G>T	XP_011533423.1:p.Val890Leu
XM_011535122.1:c.1336G>T	XP_011533424.1:p.Val446Leu
XR_941601.1:n.2887G>T
XR_941602.1:n.2887G>T
XR_941603.1:n.2887G>T
XR_941604.1:n.2887G>T
NM_001330578.1:c.2434G>T	NP_001317507.1:p.Val812Leu
NM_001330579.1:c.2416G>T	NP_001317508.1:p.Val806Leu
XM_005266424.4:c.2572G>T	XP_005266481.1:p.Val858Leu
XM_005266430.4:c.2668G>T	XP_005266487.1:p.Val890Leu
XM_005266431.4:c.2632G>T	XP_005266488.1:p.Val878Leu
XM_006719837.3:c.2572G>T	XP_006719900.1:p.Val858Leu
XM_011535117.3:c.2572G>T	XP_011533419.1:p.Val858Leu
XM_017020627.1:c.2572G>T	XP_016876116.1:p.Val858Leu
NM_000053.4:c.2668G>T MANE Select	NP_000044.2:p.Val890Leu
NM_001005918.3:c.2182G>T	NP_001005918.1:p.Val728Leu
NM_001330579.2:c.2416G>T	NP_001317508.1:p.Val806Leu
NM_001243182.2:c.2335G>T	NP_001230111.1:p.Val779Leu
NM_001330578.2:c.2434G>T	NP_001317507.1:p.Val812Leu