Canonical Allele Identifier: CA473404671

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22276960G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22255414G>A , CM000673.2:g.22255414G>A	GRCh38
NC_000011.9:g.22276960G>A , CM000673.1:g.22276960G>A	GRCh37
NC_000011.8:g.22233536G>A	NCBI36
NG_015844.1:g.67239G>A , LRG_868:g.67239G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.544G>A
ENST00000682266.1:c.774G>A	ENSP00000507766.1:p.Leu258=
ENST00000682341.1:c.1182G>A	ENSP00000508251.1:p.Leu394=
ENST00000682530.1:c.*1156G>A	ENSP00000506805.1:n.*1156G>A
ENST00000683197.1:c.1182G>A	ENSP00000507641.1:p.Leu394=
ENST00000683411.1:c.774G>A	ENSP00000508397.1:p.Leu258=
ENST00000683437.1:c.774G>A	ENSP00000508408.1:p.Leu258=
ENST00000683613.1:n.2218G>A
ENST00000683834.1:n.1424G>A
ENST00000684663.1:c.1179G>A	ENSP00000508009.1:p.Leu393=
ENST00000324559.9:c.1224G>A MANE Select	ENSP00000315371.9:p.Leu408=
ENST00000648804.1:n.1559G>A
ENST00000324559.8:c.1224G>A	ENSP00000315371.8:p.Leu408=
NM_001142649.1:c.1221G>A	NP_001136121.1:p.Leu407=
NM_213599.2:c.1224G>A , LRG_868t1:c.1224G>A	NP_998764.1:p.Leu408=
XM_005252820.2:c.1182G>A	XP_005252877.2:p.Leu394=
XM_005252821.2:c.1179G>A	XP_005252878.2:p.Leu393=
XM_005252822.3:c.1146G>A	XP_005252879.1:p.Leu382=
XM_005252823.3:c.1143G>A	XP_005252880.1:p.Leu381=
XM_011519949.1:c.1131G>A	XP_011518251.1:p.Leu377=
XM_005252820.3:c.1182G>A	XP_005252877.2:p.Leu394=
XM_005252821.3:c.1179G>A	XP_005252878.2:p.Leu393=
XM_005252822.4:c.1146G>A	XP_005252879.1:p.Leu382=
XM_011519949.2:c.1131G>A	XP_011518251.1:p.Leu377=
NM_001142649.2:c.1221G>A	NP_001136121.1:p.Leu407=
NM_213599.3:c.1224G>A MANE Select	NP_998764.1:p.Leu408=