Canonical Allele Identifier: CA1611324732
Gene: GFOD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.13370183T= , CM000668.2:g.13370183T= GRCh38
NC_000006.11:g.13370415T= , CM000668.1:g.13370415T= GRCh37
NC_000006.10:g.13478394T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379287.4:c.254-4521A= MANE Select ENSP00000368589.3:n.254-4521A=
ENST00000379284.1:c.-56-4521A= ENSP00000368586.1:n.-56-4521A=
ENST00000379287.3:c.254-4521A= ENSP00000368589.3:n.254-4521A=
ENST00000612338.4:c.-56-4521A= ENSP00000479493.1:n.-56-4521A=
NM_001242628.1:c.-56-4521A= NP_001229557.1:n.-56-4521A=
NM_001242630.1:c.-56-4521A= NP_001229559.1:n.-56-4521A=
NM_018988.3:c.254-4521A= NP_061861.1:n.254-4521A=
XM_011514699.1:c.-56-4521A= XP_011513001.1:n.-56-4521A=
XM_011514699.2:c.-56-4521A= XP_011513001.1:n.-56-4521A=
NM_018988.4:c.254-4521A= MANE Select NP_061861.1:n.254-4521A=
NM_001242628.2:c.-56-4521A= NP_001229557.1:n.-56-4521A=
NM_001242630.2:c.-56-4521A= NP_001229559.1:n.-56-4521A=