Canonical Allele Identifier: CA38977542

Gene: GNPAT

Linked Data

• dbSNP Id: rs200709360
• MyVariant Identifiers: chr1:g.231401138T>C (hg19) ; chr1:g.231265392T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231265392T>C , CM000663.2:g.231265392T>C	GRCh38
NC_000001.10:g.231401138T>C , CM000663.1:g.231401138T>C	GRCh37
NC_000001.9:g.229467761T>C	NCBI36
NG_008240.1:g.29220T>C
NG_008240.2:g.29220T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366647.9:c.668T>C MANE Select	ENSP00000355607.4:p.Phe223Ser
ENST00000644483.1:c.*354T>C	ENSP00000496537.1:n.*354T>C
ENST00000366647.8:c.668T>C	ENSP00000355607.4:p.Phe223Ser
ENST00000416000.1:c.638T>C	ENSP00000411640.1:p.Phe213Ser
ENST00000436239.5:c.485T>C	ENSP00000402811.1:p.Phe162Ser
NM_001316350.1:c.485T>C	NP_001303279.1:p.Phe162Ser
NM_014236.3:c.668T>C	NP_055051.1:p.Phe223Ser
XM_005273313.3:c.665T>C	XP_005273370.1:p.Phe222Ser
XM_011544303.1:c.341T>C	XP_011542605.1:p.Phe114Ser
XM_011544304.1:c.341T>C	XP_011542606.1:p.Phe114Ser
XM_005273313.4:c.665T>C	XP_005273370.1:p.Phe222Ser
XM_011544303.3:c.341T>C	XP_011542605.1:p.Phe114Ser
XM_011544304.2:c.341T>C	XP_011542606.1:p.Phe114Ser
NM_014236.4:c.668T>C MANE Select	NP_055051.1:p.Phe223Ser
NM_001316350.2:c.485T>C	NP_001303279.1:p.Phe162Ser