Canonical Allele Identifier: CA388025899

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52515221A>C (hg19) ; chr13:g.51941085A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941085A>C , CM000675.2:g.51941085A>C	GRCh38
NC_000013.10:g.52515221A>C , CM000675.1:g.52515221A>C	GRCh37
NC_000013.9:g.51413222A>C	NCBI36
NG_008806.1:g.75410T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1202T>G	ENSP00000489512.2:n.*1202T>G
ENST00000673864.2:c.*2296T>G	ENSP00000501045.2:n.*2296T>G
ENST00000674147.2:c.2931T>G	ENSP00000500964.2:p.Ile977Met
ENST00000242839.10:c.3552T>G MANE Select	ENSP00000242839.5:p.Ile1184Met
ENST00000344297.9:c.2931T>G	ENSP00000342559.5:p.Ile977Met
ENST00000400366.6:c.3219T>G	ENSP00000383217.3:p.Ile1073Met
ENST00000448424.7:c.3300T>G	ENSP00000416738.3:p.Ile1100Met
ENST00000673772.1:c.3318T>G	ENSP00000501168.1:p.Ile1106Met
ENST00000673867.1:n.3691T>G
ENST00000674126.1:n.3915T>G
ENST00000674147.1:c.2487T>G	ENSP00000500964.1:p.Ile829Met
ENST00000242839.8:c.3552T>G	ENSP00000242839.4:p.Ile1184Met
ENST00000344297.8:c.2931T>G	ENSP00000342559.5:p.Ile977Met
ENST00000400366.5:c.3219T>G	ENSP00000383217.3:p.Ile1073Met
ENST00000400370.8:c.2262T>G	ENSP00000383221.3:p.Ile754Met
ENST00000418097.7:c.3357T>G	ENSP00000393343.2:p.Ile1119Met
ENST00000448424.6:c.3318T>G	ENSP00000416738.2:p.Ile1106Met
ENST00000634296.1:c.1330T>G
ENST00000634308.1:c.*653T>G	ENSP00000489234.1:n.*653T>G
ENST00000634620.1:n.4296T>G
ENST00000634810.1:n.2897T>G
ENST00000634844.1:c.3408T>G	ENSP00000489398.1:p.Ile1136Met
NM_000053.3:c.3552T>G	NP_000044.2:p.Ile1184Met
NM_001005918.2:c.2931T>G	NP_001005918.1:p.Ile977Met
NM_001243182.1:c.3219T>G	NP_001230111.1:p.Ile1073Met
XM_005266423.2:c.3456T>G	XP_005266480.1:p.Ile1152Met
XM_005266424.3:c.3456T>G	XP_005266481.1:p.Ile1152Met
XM_005266427.2:c.3318T>G	XP_005266484.1:p.Ile1106Met
XM_005266428.1:c.3300T>G	XP_005266485.1:p.Ile1100Met
XM_005266430.3:c.3552T>G	XP_005266487.1:p.Ile1184Met
XM_005266431.2:c.3516T>G	XP_005266488.1:p.Ile1172Met
XM_005266432.2:c.3066T>G	XP_005266489.1:p.Ile1022Met
XM_006719837.2:c.3456T>G	XP_006719900.1:p.Ile1152Met
XM_006719838.1:c.1368T>G	XP_006719901.1:p.Ile456Met
XM_006719839.1:c.1185T>G	XP_006719902.1:p.Ile395Met
XM_011535117.1:c.3456T>G	XP_011533419.1:p.Ile1152Met
XM_011535118.1:c.3417T>G	XP_011533420.1:p.Ile1139Met
XM_011535119.1:c.3369T>G	XP_011533421.1:p.Ile1123Met
XM_011535120.1:c.3138T>G	XP_011533422.1:p.Ile1046Met
XM_011535121.1:c.3039T>G	XP_011533423.1:p.Ile1013Met
XM_011535122.1:c.2220T>G	XP_011533424.1:p.Ile740Met
XR_941601.1:n.3771T>G
XR_941602.1:n.3771T>G
XR_941603.1:n.3771T>G
XR_941604.1:n.3771T>G
NM_001330578.1:c.3318T>G	NP_001317507.1:p.Ile1106Met
NM_001330579.1:c.3300T>G	NP_001317508.1:p.Ile1100Met
XM_005266424.4:c.3456T>G	XP_005266481.1:p.Ile1152Met
XM_005266430.4:c.3552T>G	XP_005266487.1:p.Ile1184Met
XM_005266431.4:c.3516T>G	XP_005266488.1:p.Ile1172Met
XM_006719837.3:c.3456T>G	XP_006719900.1:p.Ile1152Met
XM_011535117.3:c.3456T>G	XP_011533419.1:p.Ile1152Met
XM_017020627.1:c.3456T>G	XP_016876116.1:p.Ile1152Met
NM_000053.4:c.3552T>G MANE Select	NP_000044.2:p.Ile1184Met
NM_001005918.3:c.2931T>G	NP_001005918.1:p.Ile977Met
NM_001330579.2:c.3300T>G	NP_001317508.1:p.Ile1100Met
NM_001243182.2:c.3219T>G	NP_001230111.1:p.Ile1073Met
NM_001330578.2:c.3318T>G	NP_001317507.1:p.Ile1106Met