Canonical Allele Identifier: CA379920652

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22271791A>C (hg19) ; chr11:g.22250245A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250245A>C , CM000673.2:g.22250245A>C	GRCh38
NC_000011.9:g.22271791A>C , CM000673.1:g.22271791A>C	GRCh37
NC_000011.8:g.22228367A>C	NCBI36
NG_015844.1:g.62070A>C , LRG_868:g.62070A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.207A>C
ENST00000682266.1:c.437A>C	ENSP00000507766.1:p.Tyr146Ser
ENST00000682341.1:c.845A>C	ENSP00000508251.1:p.Tyr282Ser
ENST00000682530.1:c.*819A>C	ENSP00000506805.1:n.*819A>C
ENST00000683197.1:c.845A>C	ENSP00000507641.1:p.Tyr282Ser
ENST00000683411.1:c.437A>C	ENSP00000508397.1:p.Tyr146Ser
ENST00000683437.1:c.437A>C	ENSP00000508408.1:p.Tyr146Ser
ENST00000683613.1:n.1881A>C
ENST00000683834.1:n.1087A>C
ENST00000684663.1:c.842A>C	ENSP00000508009.1:p.Tyr281Ser
ENST00000324559.9:c.887A>C MANE Select	ENSP00000315371.9:p.Tyr296Ser
ENST00000648804.1:n.1222A>C
ENST00000324559.8:c.887A>C	ENSP00000315371.8:p.Tyr296Ser
NM_001142649.1:c.884A>C	NP_001136121.1:p.Tyr295Ser
NM_213599.2:c.887A>C , LRG_868t1:c.887A>C	NP_998764.1:p.Tyr296Ser
XM_005252820.2:c.845A>C	XP_005252877.2:p.Tyr282Ser
XM_005252821.2:c.842A>C	XP_005252878.2:p.Tyr281Ser
XM_005252822.3:c.809A>C	XP_005252879.1:p.Tyr270Ser
XM_005252823.3:c.806A>C	XP_005252880.1:p.Tyr269Ser
XM_011519949.1:c.794A>C	XP_011518251.1:p.Tyr265Ser
XM_005252820.3:c.845A>C	XP_005252877.2:p.Tyr282Ser
XM_005252821.3:c.842A>C	XP_005252878.2:p.Tyr281Ser
XM_005252822.4:c.809A>C	XP_005252879.1:p.Tyr270Ser
XM_011519949.2:c.794A>C	XP_011518251.1:p.Tyr265Ser
NM_001142649.2:c.884A>C	NP_001136121.1:p.Tyr295Ser
NM_213599.3:c.887A>C MANE Select	NP_998764.1:p.Tyr296Ser