Canonical Allele Identifier: CA9293146

Gene: ANO8

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17334661C>T , CM000681.2:g.17334661C>T	GRCh38
NC_000019.9:g.17445470C>T , CM000681.1:g.17445470C>T	GRCh37
NC_000019.8:g.17306470C>T	NCBI36
NG_027824.1:g.4680C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020959.3:c.10G>A MANE Select	NP_066010.1:p.Ala4Thr
ENST00000159087.7:c.10G>A MANE Select	ENSP00000159087.4:p.Ala4Thr
NM_020959.2:c.10G>A	NP_066010.1:p.Ala4Thr
ENST00000159087.6:c.10G>A	ENSP00000159087.4:p.Ala4Thr
ENST00000597643.5:c.10G>A	ENSP00000469751.1:p.Ala4Thr
ENST00000600711.1:n.69G>A
ENST00000630631.1:c.10G>A	ENSP00000486865.1:p.Ala4Thr
XM_017027048.1:c.10G>A	XP_016882537.1:p.Ala4Thr
XR_001753729.1:n.174G>A
XR_936199.1:n.174G>A
XR_936199.3:n.169G>A
XR_936200.1:n.174G>A
XR_936201.1:n.174G>A