Canonical Allele Identifier: CA1143906829

Gene: GNPAT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231265451A= , CM000663.2:g.231265451A=	GRCh38
NC_000001.10:g.231401197A= , CM000663.1:g.231401197A=	GRCh37
NC_000001.9:g.229467820A=	NCBI36
NG_008240.1:g.29279A=
NG_008240.2:g.29279A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366647.9:c.696+31A= MANE Select	ENSP00000355607.4:n.696+31A=
ENST00000644483.1:c.*382+31A=	ENSP00000496537.1:n.*382+31A=
ENST00000366647.8:c.696+31A=	ENSP00000355607.4:n.696+31A=
ENST00000416000.1:c.666+31A=	ENSP00000411640.1:n.666+31A=
ENST00000436239.5:c.513+31A=	ENSP00000402811.1:n.513+31A=
NM_001316350.1:c.513+31A=	NP_001303279.1:n.513+31A=
NM_014236.3:c.696+31A=	NP_055051.1:n.696+31A=
XM_005273313.3:c.693+31A=	XP_005273370.1:n.693+31A=
XM_011544303.1:c.369+31A=	XP_011542605.1:n.369+31A=
XM_011544304.1:c.369+31A=	XP_011542606.1:n.369+31A=
XM_005273313.4:c.693+31A=	XP_005273370.1:n.693+31A=
XM_011544303.3:c.369+31A=	XP_011542605.1:n.369+31A=
XM_011544304.2:c.369+31A=	XP_011542606.1:n.369+31A=
NM_014236.4:c.696+31A= MANE Select	NP_055051.1:n.696+31A=
NM_001316350.2:c.513+31A=	NP_001303279.1:n.513+31A=