Canonical Allele Identifier: CA345233016

Gene: GNPAT

Linked Data

• MyVariant Identifiers: chr1:g.231401048G>T (hg19) ; chr1:g.231265302G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231265302G>T , CM000663.2:g.231265302G>T	GRCh38
NC_000001.10:g.231401048G>T , CM000663.1:g.231401048G>T	GRCh37
NC_000001.9:g.229467671G>T	NCBI36
NG_008240.1:g.29130G>T
NG_008240.2:g.29130G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366647.9:c.578G>T MANE Select	ENSP00000355607.4:p.Gly193Val
ENST00000644483.1:c.*264G>T	ENSP00000496537.1:n.*264G>T
ENST00000366647.8:c.578G>T	ENSP00000355607.4:p.Gly193Val
ENST00000416000.1:c.548G>T	ENSP00000411640.1:p.Gly183Val
ENST00000436239.5:c.395G>T	ENSP00000402811.1:p.Gly132Val
NM_001316350.1:c.395G>T	NP_001303279.1:p.Gly132Val
NM_014236.3:c.578G>T	NP_055051.1:p.Gly193Val
XM_005273313.3:c.575G>T	XP_005273370.1:p.Gly192Val
XM_011544303.1:c.251G>T	XP_011542605.1:p.Gly84Val
XM_011544304.1:c.251G>T	XP_011542606.1:p.Gly84Val
XM_005273313.4:c.575G>T	XP_005273370.1:p.Gly192Val
XM_011544303.3:c.251G>T	XP_011542605.1:p.Gly84Val
XM_011544304.2:c.251G>T	XP_011542606.1:p.Gly84Val
NM_014236.4:c.578G>T MANE Select	NP_055051.1:p.Gly193Val
NM_001316350.2:c.395G>T	NP_001303279.1:p.Gly132Val