Canonical Allele Identifier: CA345233024

Gene: GNPAT

Linked Data

• dbSNP Id: rs1685344850
• MyVariant Identifiers: chr1:g.231401050A>G (hg19) ; chr1:g.231265304A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231265304A>G , CM000663.2:g.231265304A>G	GRCh38
NC_000001.10:g.231401050A>G , CM000663.1:g.231401050A>G	GRCh37
NC_000001.9:g.229467673A>G	NCBI36
NG_008240.1:g.29132A>G
NG_008240.2:g.29132A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366647.9:c.580A>G MANE Select	ENSP00000355607.4:p.Met194Val
ENST00000644483.1:c.*266A>G	ENSP00000496537.1:n.*266A>G
ENST00000366647.8:c.580A>G	ENSP00000355607.4:p.Met194Val
ENST00000416000.1:c.550A>G	ENSP00000411640.1:p.Met184Val
ENST00000436239.5:c.397A>G	ENSP00000402811.1:p.Met133Val
NM_001316350.1:c.397A>G	NP_001303279.1:p.Met133Val
NM_014236.3:c.580A>G	NP_055051.1:p.Met194Val
XM_005273313.3:c.577A>G	XP_005273370.1:p.Met193Val
XM_011544303.1:c.253A>G	XP_011542605.1:p.Met85Val
XM_011544304.1:c.253A>G	XP_011542606.1:p.Met85Val
XM_005273313.4:c.577A>G	XP_005273370.1:p.Met193Val
XM_011544303.3:c.253A>G	XP_011542605.1:p.Met85Val
XM_011544304.2:c.253A>G	XP_011542606.1:p.Met85Val
NM_014236.4:c.580A>G MANE Select	NP_055051.1:p.Met194Val
NM_001316350.2:c.397A>G	NP_001303279.1:p.Met133Val