Canonical Allele Identifier: CA345233071

Gene: GNPAT

Linked Data

• MyVariant Identifiers: chr1:g.231401058G>A (hg19) ; chr1:g.231265312G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231265312G>A , CM000663.2:g.231265312G>A	GRCh38
NC_000001.10:g.231401058G>A , CM000663.1:g.231401058G>A	GRCh37
NC_000001.9:g.229467681G>A	NCBI36
NG_008240.1:g.29140G>A
NG_008240.2:g.29140G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366647.9:c.588G>A MANE Select	ENSP00000355607.4:p.Met196Ile
ENST00000644483.1:c.*274G>A	ENSP00000496537.1:n.*274G>A
ENST00000366647.8:c.588G>A	ENSP00000355607.4:p.Met196Ile
ENST00000416000.1:c.558G>A	ENSP00000411640.1:p.Met186Ile
ENST00000436239.5:c.405G>A	ENSP00000402811.1:p.Met135Ile
NM_001316350.1:c.405G>A	NP_001303279.1:p.Met135Ile
NM_014236.3:c.588G>A	NP_055051.1:p.Met196Ile
XM_005273313.3:c.585G>A	XP_005273370.1:p.Met195Ile
XM_011544303.1:c.261G>A	XP_011542605.1:p.Met87Ile
XM_011544304.1:c.261G>A	XP_011542606.1:p.Met87Ile
XM_005273313.4:c.585G>A	XP_005273370.1:p.Met195Ile
XM_011544303.3:c.261G>A	XP_011542605.1:p.Met87Ile
XM_011544304.2:c.261G>A	XP_011542606.1:p.Met87Ile
NM_014236.4:c.588G>A MANE Select	NP_055051.1:p.Met196Ile
NM_001316350.2:c.405G>A	NP_001303279.1:p.Met135Ile