Canonical Allele Identifier: CA388032196

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52520502G>C (hg19) ; chr13:g.51946366G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51946366G>C , CM000675.2:g.51946366G>C	GRCh38
NC_000013.10:g.52520502G>C , CM000675.1:g.52520502G>C	GRCh37
NC_000013.9:g.51418503G>C	NCBI36
NG_008806.1:g.70129C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*811C>G	ENSP00000489512.2:n.*811C>G
ENST00000673864.2:c.*1722C>G	ENSP00000501045.2:n.*1722C>G
ENST00000674147.2:c.2357C>G	ENSP00000500964.2:p.Thr786Arg
ENST00000242839.10:c.2978C>G MANE Select	ENSP00000242839.5:p.Thr993Arg
ENST00000344297.9:c.2357C>G	ENSP00000342559.5:p.Thr786Arg
ENST00000400366.6:c.2645C>G	ENSP00000383217.3:p.Thr882Arg
ENST00000448424.7:c.2726C>G	ENSP00000416738.3:p.Thr909Arg
ENST00000673772.1:c.2744C>G	ENSP00000501168.1:p.Thr915Arg
ENST00000673867.1:n.1125C>G
ENST00000674126.1:n.3341C>G
ENST00000674147.1:c.1913C>G	ENSP00000500964.1:p.Thr638Arg
ENST00000242839.8:c.2978C>G	ENSP00000242839.4:p.Thr993Arg
ENST00000344297.8:c.2357C>G	ENSP00000342559.5:p.Thr786Arg
ENST00000400366.5:c.2645C>G	ENSP00000383217.3:p.Thr882Arg
ENST00000400370.8:c.1688C>G	ENSP00000383221.3:p.Thr563Arg
ENST00000418097.7:c.2866-2075C>G	ENSP00000393343.2:n.2866-2075C>G
ENST00000448424.6:c.2744C>G	ENSP00000416738.2:p.Thr915Arg
ENST00000466629.1:n.198C>G
ENST00000634296.1:c.939C>G
ENST00000634308.1:c.*79C>G	ENSP00000489234.1:n.*79C>G
ENST00000634620.1:n.3722C>G
ENST00000634810.1:n.2323C>G
ENST00000634844.1:c.2834C>G	ENSP00000489398.1:p.Thr945Arg
ENST00000635406.1:n.324C>G
NM_000053.3:c.2978C>G	NP_000044.2:p.Thr993Arg
NM_001005918.2:c.2357C>G	NP_001005918.1:p.Thr786Arg
NM_001243182.1:c.2645C>G	NP_001230111.1:p.Thr882Arg
XM_005266423.2:c.2882C>G	XP_005266480.1:p.Thr961Arg
XM_005266424.3:c.2882C>G	XP_005266481.1:p.Thr961Arg
XM_005266427.2:c.2744C>G	XP_005266484.1:p.Thr915Arg
XM_005266428.1:c.2726C>G	XP_005266485.1:p.Thr909Arg
XM_005266430.3:c.2978C>G	XP_005266487.1:p.Thr993Arg
XM_005266431.2:c.2942C>G	XP_005266488.1:p.Thr981Arg
XM_005266432.2:c.2492C>G	XP_005266489.1:p.Thr831Arg
XM_006719837.2:c.2882C>G	XP_006719900.1:p.Thr961Arg
XM_006719838.1:c.794C>G	XP_006719901.1:p.Thr265Arg
XM_006719839.1:c.794C>G	XP_006719902.1:p.Thr265Arg
XM_011535117.1:c.2882C>G	XP_011533419.1:p.Thr961Arg
XM_011535118.1:c.2843C>G	XP_011533420.1:p.Thr948Arg
XM_011535119.1:c.2978C>G	XP_011533421.1:p.Thr993Arg
XM_011535120.1:c.2564C>G	XP_011533422.1:p.Thr855Arg
XM_011535121.1:c.2730+3641C>G	XP_011533423.1:n.2730+3641C>G
XM_011535122.1:c.1646C>G	XP_011533424.1:p.Thr549Arg
XR_941601.1:n.3197C>G
XR_941602.1:n.3197C>G
XR_941603.1:n.3197C>G
XR_941604.1:n.3197C>G
NM_001330578.1:c.2744C>G	NP_001317507.1:p.Thr915Arg
NM_001330579.1:c.2726C>G	NP_001317508.1:p.Thr909Arg
XM_005266424.4:c.2882C>G	XP_005266481.1:p.Thr961Arg
XM_005266430.4:c.2978C>G	XP_005266487.1:p.Thr993Arg
XM_005266431.4:c.2942C>G	XP_005266488.1:p.Thr981Arg
XM_006719837.3:c.2882C>G	XP_006719900.1:p.Thr961Arg
XM_011535117.3:c.2882C>G	XP_011533419.1:p.Thr961Arg
XM_017020627.1:c.2882C>G	XP_016876116.1:p.Thr961Arg
NM_000053.4:c.2978C>G MANE Select	NP_000044.2:p.Thr993Arg
NM_001005918.3:c.2357C>G	NP_001005918.1:p.Thr786Arg
NM_001330579.2:c.2726C>G	NP_001317508.1:p.Thr909Arg
NM_001243182.2:c.2645C>G	NP_001230111.1:p.Thr882Arg
NM_001330578.2:c.2744C>G	NP_001317507.1:p.Thr915Arg