Canonical Allele Identifier: CA358535002

Gene: FGG

Linked Data

• gnomAD v4: 4-154604839-A-C
• MyVariant Identifiers: chr4:g.155525991A>C (hg19) ; chr4:g.154604839A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604839A>C , CM000666.2:g.154604839A>C	GRCh38
NC_000004.11:g.155525991A>C , CM000666.1:g.155525991A>C	GRCh37
NC_000004.10:g.155745441A>C	NCBI36
NG_008834.1:g.12912T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336098.8:c.1357T>G MANE Select	ENSP00000336829.3:p.Leu453Val
ENST00000336098.7:c.1357T>G	ENSP00000336829.3:p.Leu453Val
ENST00000404648.7:c.1299+58T>G	ENSP00000384860.3:n.1299+58T>G
ENST00000405164.5:c.1323+58T>G	ENSP00000384101.1:n.1323+58T>G
ENST00000407946.5:c.1381T>G	ENSP00000384552.1:p.Leu461Val
ENST00000465913.1:n.905T>G
ENST00000492082.5:n.1841+58T>G
NM_000509.4:c.1299+58T>G	NP_000500.2:n.1299+58T>G
NM_000509.5:c.1299+58T>G	NP_000500.2:n.1299+58T>G
NM_021870.2:c.1357T>G	NP_068656.2:p.Leu453Val
NM_021870.3:c.1357T>G MANE Select	NP_068656.2:p.Leu453Val
NM_000509.6:c.1299+58T>G	NP_000500.2:n.1299+58T>G