Canonical Allele Identifier: CA1957403564

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22273230T= , CM000673.2:g.22273230T=	GRCh38
NC_000011.9:g.22294776T= , CM000673.1:g.22294776T=	GRCh37
NC_000011.8:g.22251352T=	NCBI36
NG_015844.1:g.85055T= , LRG_868:g.85055T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532043.2:n.252+241T=
ENST00000682266.1:c.1785+241T=	ENSP00000507766.1:n.1785+241T=
ENST00000682341.1:c.2193+241T=	ENSP00000508251.1:n.2193+241T=
ENST00000683197.1:c.2193+241T=	ENSP00000507641.1:n.2193+241T=
ENST00000683411.1:c.1785+241T=	ENSP00000508397.1:n.1785+241T=
ENST00000683437.1:c.1785+241T=	ENSP00000508408.1:n.1785+241T=
ENST00000683613.1:n.3229+241T=
ENST00000684663.1:c.2190+241T=	ENSP00000508009.1:n.2190+241T=
ENST00000324559.9:c.2235+241T= MANE Select	ENSP00000315371.9:n.2235+241T=
ENST00000648804.1:n.2570+241T=
ENST00000324559.8:c.2235+241T=	ENSP00000315371.8:n.2235+241T=
ENST00000532043.1:n.252+241T=
NM_001142649.1:c.2232+241T=	NP_001136121.1:n.2232+241T=
NM_213599.2:c.2235+241T= , LRG_868t1:c.2235+241T=	NP_998764.1:n.2235+241T=
XM_005252820.2:c.2193+241T=	XP_005252877.2:n.2193+241T=
XM_005252821.2:c.2190+241T=	XP_005252878.2:n.2190+241T=
XM_005252822.3:c.2157+241T=	XP_005252879.1:n.2157+241T=
XM_005252823.3:c.2154+241T=	XP_005252880.1:n.2154+241T=
XM_011519949.1:c.2142+241T=	XP_011518251.1:n.2142+241T=
XM_005252820.3:c.2193+241T=	XP_005252877.2:n.2193+241T=
XM_005252821.3:c.2190+241T=	XP_005252878.2:n.2190+241T=
XM_005252822.4:c.2157+241T=	XP_005252879.1:n.2157+241T=
XM_011519949.2:c.2142+241T=	XP_011518251.1:n.2142+241T=
NM_001142649.2:c.2232+241T=	NP_001136121.1:n.2232+241T=
NM_213599.3:c.2235+241T= MANE Select	NP_998764.1:n.2235+241T=