Canonical Allele Identifier: CA345233177

Gene: GNPAT

Linked Data

• dbSNP Id: rs1164328758
• gnomAD v4: 1-231265340-G-A
• MyVariant Identifiers: chr1:g.231401086G>A (hg19) ; chr1:g.231265340G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231265340G>A , CM000663.2:g.231265340G>A	GRCh38
NC_000001.10:g.231401086G>A , CM000663.1:g.231401086G>A	GRCh37
NC_000001.9:g.229467709G>A	NCBI36
NG_008240.1:g.29168G>A
NG_008240.2:g.29168G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366647.9:c.616G>A MANE Select	ENSP00000355607.4:p.Ala206Thr
ENST00000644483.1:c.*302G>A	ENSP00000496537.1:n.*302G>A
ENST00000366647.8:c.616G>A	ENSP00000355607.4:p.Ala206Thr
ENST00000416000.1:c.586G>A	ENSP00000411640.1:p.Ala196Thr
ENST00000436239.5:c.433G>A	ENSP00000402811.1:p.Ala145Thr
NM_001316350.1:c.433G>A	NP_001303279.1:p.Ala145Thr
NM_014236.3:c.616G>A	NP_055051.1:p.Ala206Thr
XM_005273313.3:c.613G>A	XP_005273370.1:p.Ala205Thr
XM_011544303.1:c.289G>A	XP_011542605.1:p.Ala97Thr
XM_011544304.1:c.289G>A	XP_011542606.1:p.Ala97Thr
XM_005273313.4:c.613G>A	XP_005273370.1:p.Ala205Thr
XM_011544303.3:c.289G>A	XP_011542605.1:p.Ala97Thr
XM_011544304.2:c.289G>A	XP_011542606.1:p.Ala97Thr
NM_014236.4:c.616G>A MANE Select	NP_055051.1:p.Ala206Thr
NM_001316350.2:c.433G>A	NP_001303279.1:p.Ala145Thr