Canonical Allele Identifier: CA1611324896

Gene: GFOD1

Linked Data

• dbSNP Id: rs552655

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.13370256T>G , CM000668.2:g.13370256T>G	GRCh38
NC_000006.11:g.13370488T>G , CM000668.1:g.13370488T>G	GRCh37
NC_000006.10:g.13478467T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000379287.4:c.254-4594A>C MANE Select	ENSP00000368589.3:n.254-4594A>C
ENST00000379284.1:c.-56-4594A>C	ENSP00000368586.1:n.-56-4594A>C
ENST00000379287.3:c.254-4594A>C	ENSP00000368589.3:n.254-4594A>C
ENST00000612338.4:c.-56-4594A>C	ENSP00000479493.1:n.-56-4594A>C
NM_001242628.1:c.-56-4594A>C	NP_001229557.1:n.-56-4594A>C
NM_001242630.1:c.-56-4594A>C	NP_001229559.1:n.-56-4594A>C
NM_018988.3:c.254-4594A>C	NP_061861.1:n.254-4594A>C
XM_011514699.1:c.-56-4594A>C	XP_011513001.1:n.-56-4594A>C
XM_011514699.2:c.-56-4594A>C	XP_011513001.1:n.-56-4594A>C
NM_018988.4:c.254-4594A>C MANE Select	NP_061861.1:n.254-4594A>C
NM_001242628.2:c.-56-4594A>C	NP_001229557.1:n.-56-4594A>C
NM_001242630.2:c.-56-4594A>C	NP_001229559.1:n.-56-4594A>C