Canonical Allele Identifier: CA388026687

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52515331T>C (hg19) ; chr13:g.51941195T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941195T>C , CM000675.2:g.51941195T>C	GRCh38
NC_000013.10:g.52515331T>C , CM000675.1:g.52515331T>C	GRCh37
NC_000013.9:g.51413332T>C	NCBI36
NG_008806.1:g.75300A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1092A>G	ENSP00000489512.2:n.*1092A>G
ENST00000673864.2:c.*2186A>G	ENSP00000501045.2:n.*2186A>G
ENST00000674147.2:c.2821A>G	ENSP00000500964.2:p.Ile941Val
ENST00000242839.10:c.3442A>G MANE Select	ENSP00000242839.5:p.Ile1148Val
ENST00000344297.9:c.2821A>G	ENSP00000342559.5:p.Ile941Val
ENST00000400366.6:c.3109A>G	ENSP00000383217.3:p.Ile1037Val
ENST00000448424.7:c.3190A>G	ENSP00000416738.3:p.Ile1064Val
ENST00000673772.1:c.3208A>G	ENSP00000501168.1:p.Ile1070Val
ENST00000673867.1:n.3581A>G
ENST00000674126.1:n.3805A>G
ENST00000674147.1:c.2377A>G	ENSP00000500964.1:p.Ile793Val
ENST00000242839.8:c.3442A>G	ENSP00000242839.4:p.Ile1148Val
ENST00000344297.8:c.2821A>G	ENSP00000342559.5:p.Ile941Val
ENST00000400366.5:c.3109A>G	ENSP00000383217.3:p.Ile1037Val
ENST00000400370.8:c.2152A>G	ENSP00000383221.3:p.Ile718Val
ENST00000418097.7:c.3247A>G	ENSP00000393343.2:p.Ile1083Val
ENST00000448424.6:c.3208A>G	ENSP00000416738.2:p.Ile1070Val
ENST00000634296.1:c.1220A>G
ENST00000634308.1:c.*543A>G	ENSP00000489234.1:n.*543A>G
ENST00000634620.1:n.4186A>G
ENST00000634810.1:n.2787A>G
ENST00000634844.1:c.3298A>G	ENSP00000489398.1:p.Ile1100Val
NM_000053.3:c.3442A>G	NP_000044.2:p.Ile1148Val
NM_001005918.2:c.2821A>G	NP_001005918.1:p.Ile941Val
NM_001243182.1:c.3109A>G	NP_001230111.1:p.Ile1037Val
XM_005266423.2:c.3346A>G	XP_005266480.1:p.Ile1116Val
XM_005266424.3:c.3346A>G	XP_005266481.1:p.Ile1116Val
XM_005266427.2:c.3208A>G	XP_005266484.1:p.Ile1070Val
XM_005266428.1:c.3190A>G	XP_005266485.1:p.Ile1064Val
XM_005266430.3:c.3442A>G	XP_005266487.1:p.Ile1148Val
XM_005266431.2:c.3406A>G	XP_005266488.1:p.Ile1136Val
XM_005266432.2:c.2956A>G	XP_005266489.1:p.Ile986Val
XM_006719837.2:c.3346A>G	XP_006719900.1:p.Ile1116Val
XM_006719838.1:c.1258A>G	XP_006719901.1:p.Ile420Val
XM_006719839.1:c.1075A>G	XP_006719902.1:p.Ile359Val
XM_011535117.1:c.3346A>G	XP_011533419.1:p.Ile1116Val
XM_011535118.1:c.3307A>G	XP_011533420.1:p.Ile1103Val
XM_011535119.1:c.3259A>G	XP_011533421.1:p.Ile1087Val
XM_011535120.1:c.3028A>G	XP_011533422.1:p.Ile1010Val
XM_011535121.1:c.2929A>G	XP_011533423.1:p.Ile977Val
XM_011535122.1:c.2110A>G	XP_011533424.1:p.Ile704Val
XR_941601.1:n.3661A>G
XR_941602.1:n.3661A>G
XR_941603.1:n.3661A>G
XR_941604.1:n.3661A>G
NM_001330578.1:c.3208A>G	NP_001317507.1:p.Ile1070Val
NM_001330579.1:c.3190A>G	NP_001317508.1:p.Ile1064Val
XM_005266424.4:c.3346A>G	XP_005266481.1:p.Ile1116Val
XM_005266430.4:c.3442A>G	XP_005266487.1:p.Ile1148Val
XM_005266431.4:c.3406A>G	XP_005266488.1:p.Ile1136Val
XM_006719837.3:c.3346A>G	XP_006719900.1:p.Ile1116Val
XM_011535117.3:c.3346A>G	XP_011533419.1:p.Ile1116Val
XM_017020627.1:c.3346A>G	XP_016876116.1:p.Ile1116Val
NM_000053.4:c.3442A>G MANE Select	NP_000044.2:p.Ile1148Val
NM_001005918.3:c.2821A>G	NP_001005918.1:p.Ile941Val
NM_001330579.2:c.3190A>G	NP_001317508.1:p.Ile1064Val
NM_001243182.2:c.3109A>G	NP_001230111.1:p.Ile1037Val
NM_001330578.2:c.3208A>G	NP_001317507.1:p.Ile1070Val