Canonical Allele Identifier: CA423902518

Gene: GNPAT

Linked Data

• MyVariant Identifiers: chr1:g.231401136A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231265390A>T , CM000663.2:g.231265390A>T	GRCh38
NC_000001.10:g.231401136A>T , CM000663.1:g.231401136A>T	GRCh37
NC_000001.9:g.229467759A>T	NCBI36
NG_008240.1:g.29218A>T
NG_008240.2:g.29218A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366647.9:c.666A>T MANE Select	ENSP00000355607.4:p.Val222=
ENST00000644483.1:c.*352A>T	ENSP00000496537.1:n.*352A>T
ENST00000366647.8:c.666A>T	ENSP00000355607.4:p.Val222=
ENST00000416000.1:c.636A>T	ENSP00000411640.1:p.Val212=
ENST00000436239.5:c.483A>T	ENSP00000402811.1:p.Val161=
NM_001316350.1:c.483A>T	NP_001303279.1:p.Val161=
NM_014236.3:c.666A>T	NP_055051.1:p.Val222=
XM_005273313.3:c.663A>T	XP_005273370.1:p.Val221=
XM_011544303.1:c.339A>T	XP_011542605.1:p.Val113=
XM_011544304.1:c.339A>T	XP_011542606.1:p.Val113=
XM_005273313.4:c.663A>T	XP_005273370.1:p.Val221=
XM_011544303.3:c.339A>T	XP_011542605.1:p.Val113=
XM_011544304.2:c.339A>T	XP_011542606.1:p.Val113=
NM_014236.4:c.666A>T MANE Select	NP_055051.1:p.Val222=
NM_001316350.2:c.483A>T	NP_001303279.1:p.Val161=