Canonical Allele Identifier: CA388034782

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52524254A>C (hg19) ; chr13:g.51950118A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51950118A>C , CM000675.2:g.51950118A>C	GRCh38
NC_000013.10:g.52524254A>C , CM000675.1:g.52524254A>C	GRCh37
NC_000013.9:g.51422255A>C	NCBI36
NG_008806.1:g.66377T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*452T>G	ENSP00000489512.2:n.*452T>G
ENST00000673864.2:c.*1363T>G	ENSP00000501045.2:n.*1363T>G
ENST00000674147.2:c.2133T>G	ENSP00000500964.2:p.Ile711Met
ENST00000242839.10:c.2619T>G MANE Select	ENSP00000242839.5:p.Ile873Met
ENST00000344297.9:c.2133T>G	ENSP00000342559.5:p.Ile711Met
ENST00000400366.6:c.2286T>G	ENSP00000383217.3:p.Ile762Met
ENST00000448424.7:c.2367T>G	ENSP00000416738.3:p.Ile789Met
ENST00000673772.1:c.2385T>G	ENSP00000501168.1:p.Ile795Met
ENST00000674147.1:c.1689T>G	ENSP00000500964.1:p.Ile563Met
ENST00000242839.8:c.2619T>G	ENSP00000242839.4:p.Ile873Met
ENST00000344297.8:c.2133T>G	ENSP00000342559.5:p.Ile711Met
ENST00000400366.5:c.2286T>G	ENSP00000383217.3:p.Ile762Met
ENST00000400370.8:c.1329T>G	ENSP00000383221.3:p.Ile443Met
ENST00000418097.7:c.2619T>G	ENSP00000393343.2:p.Ile873Met
ENST00000448424.6:c.2385T>G	ENSP00000416738.2:p.Ile795Met
ENST00000634296.1:c.580T>G
ENST00000634308.1:c.2385T>G	ENSP00000489234.1:p.Ile795Met
ENST00000634620.1:n.3417T>G
ENST00000634810.1:n.1964T>G
ENST00000634844.1:c.2475T>G	ENSP00000489398.1:p.Ile825Met
ENST00000635406.1:n.212-3640T>G
NM_000053.3:c.2619T>G	NP_000044.2:p.Ile873Met
NM_001005918.2:c.2133T>G	NP_001005918.1:p.Ile711Met
NM_001243182.1:c.2286T>G	NP_001230111.1:p.Ile762Met
XM_005266423.2:c.2523T>G	XP_005266480.1:p.Ile841Met
XM_005266424.3:c.2523T>G	XP_005266481.1:p.Ile841Met
XM_005266427.2:c.2385T>G	XP_005266484.1:p.Ile795Met
XM_005266428.1:c.2367T>G	XP_005266485.1:p.Ile789Met
XM_005266430.3:c.2619T>G	XP_005266487.1:p.Ile873Met
XM_005266431.2:c.2583T>G	XP_005266488.1:p.Ile861Met
XM_005266432.2:c.2133T>G	XP_005266489.1:p.Ile711Met
XM_006719837.2:c.2523T>G	XP_006719900.1:p.Ile841Met
XM_006719838.1:c.435T>G	XP_006719901.1:p.Ile145Met
XM_006719839.1:c.435T>G	XP_006719902.1:p.Ile145Met
XM_011535117.1:c.2523T>G	XP_011533419.1:p.Ile841Met
XM_011535118.1:c.2619T>G	XP_011533420.1:p.Ile873Met
XM_011535119.1:c.2619T>G	XP_011533421.1:p.Ile873Met
XM_011535120.1:c.2205T>G	XP_011533422.1:p.Ile735Met
XM_011535121.1:c.2619T>G	XP_011533423.1:p.Ile873Met
XM_011535122.1:c.1287T>G	XP_011533424.1:p.Ile429Met
XR_941601.1:n.2838T>G
XR_941602.1:n.2838T>G
XR_941603.1:n.2838T>G
XR_941604.1:n.2838T>G
NM_001330578.1:c.2385T>G	NP_001317507.1:p.Ile795Met
NM_001330579.1:c.2367T>G	NP_001317508.1:p.Ile789Met
XM_005266424.4:c.2523T>G	XP_005266481.1:p.Ile841Met
XM_005266430.4:c.2619T>G	XP_005266487.1:p.Ile873Met
XM_005266431.4:c.2583T>G	XP_005266488.1:p.Ile861Met
XM_006719837.3:c.2523T>G	XP_006719900.1:p.Ile841Met
XM_011535117.3:c.2523T>G	XP_011533419.1:p.Ile841Met
XM_017020627.1:c.2523T>G	XP_016876116.1:p.Ile841Met
NM_000053.4:c.2619T>G MANE Select	NP_000044.2:p.Ile873Met
NM_001005918.3:c.2133T>G	NP_001005918.1:p.Ile711Met
NM_001330579.2:c.2367T>G	NP_001317508.1:p.Ile789Met
NM_001243182.2:c.2286T>G	NP_001230111.1:p.Ile762Met
NM_001330578.2:c.2385T>G	NP_001317507.1:p.Ile795Met