Canonical Allele Identifier: CA6988637

Gene: ATP7B

Linked Data

• dbSNP Id: rs761310545
• ExAC: 13:52513327 C / T
• gnomAD v2: 13-52513327-C-T
• gnomAD v4: 13-51939191-C-T
• MyVariant Identifiers: chr13:g.52513327C>T (hg19) ; chr13:g.51939191C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51939191C>T , CM000675.2:g.51939191C>T	GRCh38
NC_000013.10:g.52513327C>T , CM000675.1:g.52513327C>T	GRCh37
NC_000013.9:g.51411328C>T	NCBI36
NG_008806.1:g.77304G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1209G>A	ENSP00000489512.2:n.*1209G>A
ENST00000673864.2:c.*2303G>A	ENSP00000501045.2:n.*2303G>A
ENST00000674147.2:c.2938G>A	ENSP00000500964.2:p.Val980Met
ENST00000242839.10:c.3559G>A MANE Select	ENSP00000242839.5:p.Val1187Met
ENST00000344297.9:c.2938G>A	ENSP00000342559.5:p.Val980Met
ENST00000400366.6:c.3226G>A	ENSP00000383217.3:p.Val1076Met
ENST00000448424.7:c.3307G>A	ENSP00000416738.3:p.Val1103Met
ENST00000673696.1:n.800G>A
ENST00000673772.1:c.3325G>A	ENSP00000501168.1:p.Val1109Met
ENST00000673867.1:n.3698G>A
ENST00000673923.1:n.425G>A
ENST00000674147.1:c.2494G>A	ENSP00000500964.1:p.Val832Met
ENST00000242839.8:c.3559G>A	ENSP00000242839.4:p.Val1187Met
ENST00000344297.8:c.2938G>A	ENSP00000342559.5:p.Val980Met
ENST00000400366.5:c.3226G>A	ENSP00000383217.3:p.Val1076Met
ENST00000400370.8:c.2269G>A	ENSP00000383221.3:p.Val757Met
ENST00000418097.7:c.3364G>A	ENSP00000393343.2:p.Val1122Met
ENST00000448424.6:c.3325G>A	ENSP00000416738.2:p.Val1109Met
ENST00000634296.1:c.1337G>A
ENST00000634308.1:c.*660G>A	ENSP00000489234.1:n.*660G>A
ENST00000634620.1:n.4303G>A
ENST00000634810.1:n.2904G>A
ENST00000634844.1:c.3415G>A	ENSP00000489398.1:p.Val1139Met
NM_000053.3:c.3559G>A	NP_000044.2:p.Val1187Met
NM_001005918.2:c.2938G>A	NP_001005918.1:p.Val980Met
NM_001243182.1:c.3226G>A	NP_001230111.1:p.Val1076Met
XM_005266423.2:c.3463G>A	XP_005266480.1:p.Val1155Met
XM_005266424.3:c.3463G>A	XP_005266481.1:p.Val1155Met
XM_005266427.2:c.3325G>A	XP_005266484.1:p.Val1109Met
XM_005266428.1:c.3307G>A	XP_005266485.1:p.Val1103Met
XM_005266430.3:c.3559G>A	XP_005266487.1:p.Val1187Met
XM_005266431.2:c.3523G>A	XP_005266488.1:p.Val1175Met
XM_005266432.2:c.3073G>A	XP_005266489.1:p.Val1025Met
XM_006719837.2:c.3463G>A	XP_006719900.1:p.Val1155Met
XM_006719838.1:c.1375G>A	XP_006719901.1:p.Val459Met
XM_006719839.1:c.1192G>A	XP_006719902.1:p.Val398Met
XM_011535117.1:c.3463G>A	XP_011533419.1:p.Val1155Met
XM_011535118.1:c.3424G>A	XP_011533420.1:p.Val1142Met
XM_011535119.1:c.3376G>A	XP_011533421.1:p.Val1126Met
XM_011535120.1:c.3145G>A	XP_011533422.1:p.Val1049Met
XM_011535121.1:c.3046G>A	XP_011533423.1:p.Val1016Met
XM_011535122.1:c.2227G>A	XP_011533424.1:p.Val743Met
XR_941601.1:n.3778G>A
XR_941602.1:n.3778G>A
XR_941603.1:n.3778G>A
XR_941604.1:n.3778G>A
NM_001330578.1:c.3325G>A	NP_001317507.1:p.Val1109Met
NM_001330579.1:c.3307G>A	NP_001317508.1:p.Val1103Met
XM_005266424.4:c.3463G>A	XP_005266481.1:p.Val1155Met
XM_005266430.4:c.3559G>A	XP_005266487.1:p.Val1187Met
XM_005266431.4:c.3523G>A	XP_005266488.1:p.Val1175Met
XM_006719837.3:c.3463G>A	XP_006719900.1:p.Val1155Met
XM_011535117.3:c.3463G>A	XP_011533419.1:p.Val1155Met
XM_017020627.1:c.3463G>A	XP_016876116.1:p.Val1155Met
NM_000053.4:c.3559G>A MANE Select	NP_000044.2:p.Val1187Met
NM_001005918.3:c.2938G>A	NP_001005918.1:p.Val980Met
NM_001330579.2:c.3307G>A	NP_001317508.1:p.Val1103Met
NM_001243182.2:c.3226G>A	NP_001230111.1:p.Val1076Met
NM_001330578.2:c.3325G>A	NP_001317507.1:p.Val1109Met