Canonical Allele Identifier: CA2640213619

Gene: CANT1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78992538G>A , CM000679.2:g.78992538G>A	GRCh38
NC_000017.10:g.76988620G>A , CM000679.1:g.76988620G>A	GRCh37
NC_000017.9:g.74500215G>A	NCBI36
NG_016645.1:g.22280C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001159773.2:c.*1012C>T MANE Select	NP_001153245.1:n.*1012C>T
ENST00000392446.10:c.*1012C>T MANE Select	ENSP00000376241.4:n.*1012C>T
NM_001159772.1:c.*1012C>T	NP_001153244.1:n.*1012C>T
NM_001159772.2:c.*1012C>T	NP_001153244.1:n.*1012C>T
NM_001159773.1:c.*1012C>T	NP_001153245.1:n.*1012C>T
NM_138793.3:c.*1012C>T	NP_620148.1:n.*1012C>T
NM_138793.4:c.*1012C>T	NP_620148.1:n.*1012C>T
ENST00000302345.6:c.*1012C>T	ENSP00000307674.2:n.*1012C>T
ENST00000392446.9:c.*1012C>T	ENSP00000376241.4:n.*1012C>T
ENST00000592228.1:c.*76C>T	ENSP00000466743.1:n.*76C>T
ENST00000620915.4:c.*1012C>T	ENSP00000477798.1:n.*1012C>T
XM_005257020.1:c.*1012C>T	XP_005257077.1:n.*1012C>T
XM_005257021.1:c.*1012C>T	XP_005257078.1:n.*1012C>T
XM_005257022.1:c.*1012C>T	XP_005257079.1:n.*1012C>T
XM_006721683.1:c.*1012C>T	XP_006721746.1:n.*1012C>T
XM_011524291.1:c.*1012C>T	XP_011522593.1:n.*1012C>T
XM_011524292.1:c.*1012C>T	XP_011522594.1:n.*1012C>T
XM_011524293.1:c.*1012C>T	XP_011522595.1:n.*1012C>T
XM_011524294.1:c.*1012C>T	XP_011522596.1:n.*1012C>T
XM_011524294.2:c.*1012C>T	XP_011522596.1:n.*1012C>T
XM_011524295.1:c.*1012C>T	XP_011522597.1:n.*1012C>T
XM_011524295.2:c.*1012C>T	XP_011522597.1:n.*1012C>T
XM_024450564.1:c.*1012C>T	XP_024306332.1:n.*1012C>T
XR_001752424.2:n.2662C>T
XR_935009.1:n.2433G>A