Canonical Allele Identifier: CA1226898702

Gene: GNPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231265284C= , CM000663.2:g.231265284C=	GRCh38
NC_000001.10:g.231401030C= , CM000663.1:g.231401030C=	GRCh37
NC_000001.9:g.229467653C=	NCBI36
NG_008240.1:g.29112C=
NG_008240.2:g.29112C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366647.9:c.569-9C= MANE Select	ENSP00000355607.4:n.569-9C=
ENST00000644483.1:c.*255-9C=	ENSP00000496537.1:n.*255-9C=
ENST00000366647.8:c.569-9C=	ENSP00000355607.4:n.569-9C=
ENST00000416000.1:c.539-9C=	ENSP00000411640.1:n.539-9C=
ENST00000436239.5:c.386-9C=	ENSP00000402811.1:n.386-9C=
NM_001316350.1:c.386-9C=	NP_001303279.1:n.386-9C=
NM_014236.3:c.569-9C=	NP_055051.1:n.569-9C=
XM_005273313.3:c.566-9C=	XP_005273370.1:n.566-9C=
XM_011544303.1:c.242-9C=	XP_011542605.1:n.242-9C=
XM_011544304.1:c.242-9C=	XP_011542606.1:n.242-9C=
XM_005273313.4:c.566-9C=	XP_005273370.1:n.566-9C=
XM_011544303.3:c.242-9C=	XP_011542605.1:n.242-9C=
XM_011544304.2:c.242-9C=	XP_011542606.1:n.242-9C=
NM_014236.4:c.569-9C= MANE Select	NP_055051.1:n.569-9C=
NM_001316350.2:c.386-9C=	NP_001303279.1:n.386-9C=