Canonical Allele Identifier: CA1140265697

Gene: GNPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231272345A= , CM000663.2:g.231272345A=	GRCh38
NC_000001.10:g.231408091A= , CM000663.1:g.231408091A=	GRCh37
NC_000001.9:g.229474714A=	NCBI36
NG_008240.1:g.36173A=
NG_008240.2:g.36173A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366647.9:c.1556A= MANE Select	ENSP00000355607.4:p.Asp519=
ENST00000644483.1:c.*1242A=	ENSP00000496537.1:n.*1242A=
ENST00000366647.8:c.1556A=	ENSP00000355607.4:p.Asp519=
ENST00000416000.1:c.1526A=	ENSP00000411640.1:p.Asp509=
NM_001316350.1:c.1373A=	NP_001303279.1:p.Asp458=
NM_014236.3:c.1556A=	NP_055051.1:p.Asp519=
XM_005273313.3:c.1553A=	XP_005273370.1:p.Asp518=
XM_011544303.1:c.1229A=	XP_011542605.1:p.Asp410=
XM_011544304.1:c.1229A=	XP_011542606.1:p.Asp410=
XM_005273313.4:c.1553A=	XP_005273370.1:p.Asp518=
XM_011544303.3:c.1229A=	XP_011542605.1:p.Asp410=
XM_011544304.2:c.1229A=	XP_011542606.1:p.Asp410=
NM_014236.4:c.1556A= MANE Select	NP_055051.1:p.Asp519=
NM_001316350.2:c.1373A=	NP_001303279.1:p.Asp458=