Canonical Allele Identifier: CA49510483
Community Standard Title: NM_001244710.2(GFPT1):c.1204-111C>T
Gene: GFPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.69338676G>A , CM000664.2:g.69338676G>A GRCh38
NC_000002.11:g.69565808G>A , CM000664.1:g.69565808G>A GRCh37
NC_000002.10:g.69419312G>A NCBI36
NG_029542.1:g.53575C>T , LRG_787:g.53575C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001244710.2:c.1204-111C>T MANE Select NP_001231639.1:n.1204-111C>T
ENST00000357308.9:c.1204-111C>T MANE Select ENSP00000349860.4:n.1204-111C>T
NM_001244710.1:c.1204-111C>T , LRG_787t1:c.1204-111C>T NP_001231639.1:n.1204-111C>T
NM_002056.3:c.1150-111C>T NP_002047.2:n.1150-111C>T
NM_002056.4:c.1150-111C>T NP_002047.2:n.1150-111C>T
ENST00000357308.8:c.1204-111C>T ENSP00000349860.4:n.1204-111C>T
ENST00000361060.5:c.1150-111C>T ENSP00000354347.4:n.1150-111C>T
ENST00000674438.1:c.934-111C>T ENSP00000501469.1:n.934-111C>T
ENST00000674507.1:c.1150-111C>T ENSP00000501332.1:n.1150-111C>T
XM_017003801.1:c.1279-111C>T XP_016859290.1:n.1279-111C>T
XM_017003802.2:c.1225-111C>T XP_016859291.1:n.1225-111C>T