Canonical Allele Identifier: CA1693558
Gene: GFPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.69328285C>T , CM000664.2:g.69328285C>T GRCh38
NC_000002.11:g.69555417C>T , CM000664.1:g.69555417C>T GRCh37
NC_000002.10:g.69408921C>T NCBI36
NG_029542.1:g.63966G>A , LRG_787:g.63966G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001244710.2:c.1879G>A MANE Select NP_001231639.1:p.Val627Met
ENST00000357308.9:c.1879G>A MANE Select ENSP00000349860.4:p.Val627Met
NM_001244710.1:c.1879G>A , LRG_787t1:c.1879G>A NP_001231639.1:p.Val627Met
NM_002056.3:c.1825G>A NP_002047.2:p.Val609Met
NM_002056.4:c.1825G>A NP_002047.2:p.Val609Met
ENST00000357308.8:c.1879G>A ENSP00000349860.4:p.Val627Met
ENST00000361060.5:c.1825G>A ENSP00000354347.4:p.Val609Met
ENST00000674438.1:c.1609G>A ENSP00000501469.1:p.Val537Met
ENST00000674507.1:c.1671+1012G>A ENSP00000501332.1:n.1671+1012G>A
XM_017003801.1:c.1954G>A XP_016859290.1:p.Val652Met
XM_017003802.2:c.1900G>A XP_016859291.1:p.Val634Met