Canonical Allele Identifier: CA1957416954

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22255504A= , CM000673.2:g.22255504A=	GRCh38
NC_000011.9:g.22277050A= , CM000673.1:g.22277050A=	GRCh37
NC_000011.8:g.22233626A=	NCBI36
NG_015844.1:g.67329A= , LRG_868:g.67329A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.634A=
ENST00000682266.1:c.864A=	ENSP00000507766.1:p.Lys288=
ENST00000682341.1:c.1272A=	ENSP00000508251.1:p.Lys424=
ENST00000682530.1:c.*1246A=	ENSP00000506805.1:n.*1246A=
ENST00000683197.1:c.1272A=	ENSP00000507641.1:p.Lys424=
ENST00000683411.1:c.864A=	ENSP00000508397.1:p.Lys288=
ENST00000683437.1:c.864A=	ENSP00000508408.1:p.Lys288=
ENST00000683613.1:n.2308A=
ENST00000683834.1:n.1514A=
ENST00000684663.1:c.1269A=	ENSP00000508009.1:p.Lys423=
ENST00000324559.9:c.1314A= MANE Select	ENSP00000315371.9:p.Lys438=
ENST00000648804.1:n.1649A=
ENST00000324559.8:c.1314A=	ENSP00000315371.8:p.Lys438=
NM_001142649.1:c.1311A=	NP_001136121.1:p.Lys437=
NM_213599.2:c.1314A= , LRG_868t1:c.1314A=	NP_998764.1:p.Lys438=
XM_005252820.2:c.1272A=	XP_005252877.2:p.Lys424=
XM_005252821.2:c.1269A=	XP_005252878.2:p.Lys423=
XM_005252822.3:c.1236A=	XP_005252879.1:p.Lys412=
XM_005252823.3:c.1233A=	XP_005252880.1:p.Lys411=
XM_011519949.1:c.1221A=	XP_011518251.1:p.Lys407=
XM_005252820.3:c.1272A=	XP_005252877.2:p.Lys424=
XM_005252821.3:c.1269A=	XP_005252878.2:p.Lys423=
XM_005252822.4:c.1236A=	XP_005252879.1:p.Lys412=
XM_011519949.2:c.1221A=	XP_011518251.1:p.Lys407=
NM_001142649.2:c.1311A=	NP_001136121.1:p.Lys437=
NM_213599.3:c.1314A= MANE Select	NP_998764.1:p.Lys438=