Canonical Allele Identifier: CA12225328

Gene: GFOD1

Linked Data

• dbSNP Id: rs552655
• gnomAD v2: 6-13370488-T-C
• gnomAD v3: 6-13370256-T-C
• gnomAD v4: 6-13370256-T-C
• MyVariant Identifiers: chr6:g.13370488T>C (hg19) ; chr6:g.13370256T>C (hg38)

Genomic Alleles

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

Transcript Alleles

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