Canonical Allele Identifier: CA345233203

Gene: GNPAT

Linked Data

• MyVariant Identifiers: chr1:g.231401092T>A (hg19) ; chr1:g.231265346T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231265346T>A , CM000663.2:g.231265346T>A	GRCh38
NC_000001.10:g.231401092T>A , CM000663.1:g.231401092T>A	GRCh37
NC_000001.9:g.229467715T>A	NCBI36
NG_008240.1:g.29174T>A
NG_008240.2:g.29174T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366647.9:c.622T>A MANE Select	ENSP00000355607.4:p.Phe208Ile
ENST00000644483.1:c.*308T>A	ENSP00000496537.1:n.*308T>A
ENST00000366647.8:c.622T>A	ENSP00000355607.4:p.Phe208Ile
ENST00000416000.1:c.592T>A	ENSP00000411640.1:p.Phe198Ile
ENST00000436239.5:c.439T>A	ENSP00000402811.1:p.Phe147Ile
NM_001316350.1:c.439T>A	NP_001303279.1:p.Phe147Ile
NM_014236.3:c.622T>A	NP_055051.1:p.Phe208Ile
XM_005273313.3:c.619T>A	XP_005273370.1:p.Phe207Ile
XM_011544303.1:c.295T>A	XP_011542605.1:p.Phe99Ile
XM_011544304.1:c.295T>A	XP_011542606.1:p.Phe99Ile
XM_005273313.4:c.619T>A	XP_005273370.1:p.Phe207Ile
XM_011544303.3:c.295T>A	XP_011542605.1:p.Phe99Ile
XM_011544304.2:c.295T>A	XP_011542606.1:p.Phe99Ile
NM_014236.4:c.622T>A MANE Select	NP_055051.1:p.Phe208Ile
NM_001316350.2:c.439T>A	NP_001303279.1:p.Phe147Ile