Canonical Allele Identifier: CA358536074

Gene: FGG

Linked Data

• gnomAD v4: 4-154606945-C-T
• MyVariant Identifiers: chr4:g.155528097C>T (hg19) ; chr4:g.154606945C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154606945C>T , CM000666.2:g.154606945C>T	GRCh38
NC_000004.11:g.155528097C>T , CM000666.1:g.155528097C>T	GRCh37
NC_000004.10:g.155747547C>T	NCBI36
NG_008834.1:g.10806G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336098.8:c.889G>A MANE Select	ENSP00000336829.3:p.Ala297Thr
ENST00000336098.7:c.889G>A	ENSP00000336829.3:p.Ala297Thr
ENST00000404648.7:c.889G>A	ENSP00000384860.3:p.Ala297Thr
ENST00000405164.5:c.913G>A	ENSP00000384101.1:p.Ala305Thr
ENST00000407946.5:c.913G>A	ENSP00000384552.1:p.Ala305Thr
ENST00000465913.1:n.437G>A
ENST00000492082.5:n.1431G>A
NM_000509.4:c.889G>A	NP_000500.2:p.Ala297Thr
NM_000509.5:c.889G>A	NP_000500.2:p.Ala297Thr
NM_021870.2:c.889G>A	NP_068656.2:p.Ala297Thr
NM_021870.3:c.889G>A MANE Select	NP_068656.2:p.Ala297Thr
NM_000509.6:c.889G>A	NP_000500.2:p.Ala297Thr