Canonical Allele Identifier: CA8808792

Gene: CANT1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78997429G>A , CM000679.2:g.78997429G>A	GRCh38
NC_000017.10:g.76993511G>A , CM000679.1:g.76993511G>A	GRCh37
NC_000017.9:g.74505106G>A	NCBI36
NG_016645.1:g.17389C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001159773.2:c.194C>T MANE Select	NP_001153245.1:p.Ala65Val
ENST00000392446.10:c.194C>T MANE Select	ENSP00000376241.4:p.Ala65Val
NM_001159772.1:c.194C>T	NP_001153244.1:p.Ala65Val
NM_001159772.2:c.194C>T	NP_001153244.1:p.Ala65Val
NM_001159773.1:c.194C>T	NP_001153245.1:p.Ala65Val
NM_138793.3:c.194C>T	NP_620148.1:p.Ala65Val
NM_138793.4:c.194C>T	NP_620148.1:p.Ala65Val
ENST00000302345.6:c.194C>T	ENSP00000307674.2:p.Ala65Val
ENST00000392446.9:c.194C>T	ENSP00000376241.4:p.Ala65Val
ENST00000588075.5:c.194C>T	ENSP00000465769.1:p.Ala65Val
ENST00000588611.5:c.132+62C>T	ENSP00000465816.1:n.132+62C>T
ENST00000590370.5:c.194C>T	ENSP00000466637.1:p.Ala65Val
ENST00000591773.5:c.194C>T	ENSP00000467437.1:p.Ala65Val
ENST00000592228.1:c.194C>T	ENSP00000466743.1:p.Ala65Val
ENST00000620915.4:c.194C>T	ENSP00000477798.1:p.Ala65Val
XM_005257020.1:c.194C>T	XP_005257077.1:p.Ala65Val
XM_005257021.1:c.194C>T	XP_005257078.1:p.Ala65Val
XM_005257022.1:c.194C>T	XP_005257079.1:p.Ala65Val
XM_006721683.1:c.194C>T	XP_006721746.1:p.Ala65Val
XM_011524291.1:c.194C>T	XP_011522593.1:p.Ala65Val
XM_011524292.1:c.194C>T	XP_011522594.1:p.Ala65Val
XM_011524293.1:c.194C>T	XP_011522595.1:p.Ala65Val
XM_011524294.1:c.194C>T	XP_011522596.1:p.Ala65Val
XM_011524294.2:c.194C>T	XP_011522596.1:p.Ala65Val
XM_011524295.1:c.194C>T	XP_011522597.1:p.Ala65Val
XM_011524295.2:c.194C>T	XP_011522597.1:p.Ala65Val
XM_024450564.1:c.194C>T	XP_024306332.1:p.Ala65Val
XR_001752424.2:n.638C>T