Canonical Allele Identifier: CA441820236

Gene: FGG

Linked Data

• MyVariant Identifiers: chr4:g.155533579A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154612427A>G , CM000666.2:g.154612427A>G	GRCh38
NC_000004.11:g.155533579A>G , CM000666.1:g.155533579A>G	GRCh37
NC_000004.10:g.155753029A>G	NCBI36
NG_008834.1:g.5324T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.87T>C MANE Select	ENSP00000336829.3:p.Ala29=
ENST00000336098.7:c.87T>C	ENSP00000336829.3:p.Ala29=
ENST00000393846.6:c.-223T>C	ENSP00000377429.2:n.-223T>C
ENST00000404648.7:c.87T>C	ENSP00000384860.3:p.Ala29=
ENST00000405164.5:c.87T>C	ENSP00000384101.1:p.Ala29=
ENST00000407946.5:c.87T>C	ENSP00000384552.1:p.Ala29=
ENST00000443553.5:c.-189T>C	ENSP00000407562.1:n.-189T>C
ENST00000464532.5:n.134T>C
ENST00000465336.1:n.134T>C
ENST00000473393.5:n.113T>C
ENST00000484695.1:n.89T>C
ENST00000492082.5:n.137T>C
NM_000509.4:c.87T>C	NP_000500.2:p.Ala29=
NM_000509.5:c.87T>C	NP_000500.2:p.Ala29=
NM_021870.2:c.87T>C	NP_068656.2:p.Ala29=
NM_021870.3:c.87T>C MANE Select	NP_068656.2:p.Ala29=
NM_000509.6:c.87T>C	NP_000500.2:p.Ala29=