Canonical Allele Identifier: CA379925410

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22301267A>T (hg19) ; chr11:g.22279721A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22279721A>T , CM000673.2:g.22279721A>T	GRCh38
NC_000011.9:g.22301267A>T , CM000673.1:g.22301267A>T	GRCh37
NC_000011.8:g.22257843A>T	NCBI36
NG_015844.1:g.91546A>T , LRG_868:g.91546A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.2248A>T	ENSP00000507766.1:p.Met750Leu
ENST00000682341.1:c.2656A>T	ENSP00000508251.1:p.Met886Leu
ENST00000683197.1:c.*162A>T	ENSP00000507641.1:n.*162A>T
ENST00000683411.1:c.2248A>T	ENSP00000508397.1:p.Met750Leu
ENST00000683437.1:c.2248A>T	ENSP00000508408.1:p.Met750Leu
ENST00000683613.1:n.3692A>T
ENST00000684663.1:c.2653A>T	ENSP00000508009.1:p.Met885Leu
ENST00000324559.9:c.2698A>T MANE Select	ENSP00000315371.9:p.Met900Leu
ENST00000648804.1:n.3033A>T
ENST00000324559.8:c.2698A>T	ENSP00000315371.8:p.Met900Leu
NM_001142649.1:c.2695A>T	NP_001136121.1:p.Met899Leu
NM_213599.2:c.2698A>T , LRG_868t1:c.2698A>T	NP_998764.1:p.Met900Leu
XM_005252820.2:c.2656A>T	XP_005252877.2:p.Met886Leu
XM_005252821.2:c.2653A>T	XP_005252878.2:p.Met885Leu
XM_005252822.3:c.2620A>T	XP_005252879.1:p.Met874Leu
XM_005252823.3:c.2617A>T	XP_005252880.1:p.Met873Leu
XM_011519949.1:c.2605A>T	XP_011518251.1:p.Met869Leu
XM_005252820.3:c.2656A>T	XP_005252877.2:p.Met886Leu
XM_005252821.3:c.2653A>T	XP_005252878.2:p.Met885Leu
XM_005252822.4:c.2620A>T	XP_005252879.1:p.Met874Leu
XM_011519949.2:c.2605A>T	XP_011518251.1:p.Met869Leu
NM_001142649.2:c.2695A>T	NP_001136121.1:p.Met899Leu
NM_213599.3:c.2698A>T MANE Select	NP_998764.1:p.Met900Leu