Canonical Allele Identifier: CA473407318

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22284512T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262966T>C , CM000673.2:g.22262966T>C	GRCh38
NC_000011.9:g.22284512T>C , CM000673.1:g.22284512T>C	GRCh37
NC_000011.8:g.22241088T>C	NCBI36
NG_015844.1:g.74791T>C , LRG_868:g.74791T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1371T>C	ENSP00000507766.1:p.Leu457=
ENST00000682341.1:c.1779T>C	ENSP00000508251.1:p.Leu593=
ENST00000683197.1:c.1779T>C	ENSP00000507641.1:p.Leu593=
ENST00000683411.1:c.1371T>C	ENSP00000508397.1:p.Leu457=
ENST00000683437.1:c.1371T>C	ENSP00000508408.1:p.Leu457=
ENST00000683613.1:n.2815T>C
ENST00000684663.1:c.1776T>C	ENSP00000508009.1:p.Leu592=
ENST00000324559.9:c.1821T>C MANE Select	ENSP00000315371.9:p.Leu607=
ENST00000648804.1:n.2156T>C
ENST00000324559.8:c.1821T>C	ENSP00000315371.8:p.Leu607=
NM_001142649.1:c.1818T>C	NP_001136121.1:p.Leu606=
NM_213599.2:c.1821T>C , LRG_868t1:c.1821T>C	NP_998764.1:p.Leu607=
XM_005252820.2:c.1779T>C	XP_005252877.2:p.Leu593=
XM_005252821.2:c.1776T>C	XP_005252878.2:p.Leu592=
XM_005252822.3:c.1743T>C	XP_005252879.1:p.Leu581=
XM_005252823.3:c.1740T>C	XP_005252880.1:p.Leu580=
XM_011519949.1:c.1728T>C	XP_011518251.1:p.Leu576=
XM_005252820.3:c.1779T>C	XP_005252877.2:p.Leu593=
XM_005252821.3:c.1776T>C	XP_005252878.2:p.Leu592=
XM_005252822.4:c.1743T>C	XP_005252879.1:p.Leu581=
XM_011519949.2:c.1728T>C	XP_011518251.1:p.Leu576=
NM_001142649.2:c.1818T>C	NP_001136121.1:p.Leu606=
NM_213599.3:c.1821T>C MANE Select	NP_998764.1:p.Leu607=