Canonical Allele Identifier: CA1504952260

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604928_154604931delinsCCTT , CM000666.2:g.154604928_154604931delinsCCTT	GRCh38
NC_000004.11:g.155526080_155526083delinsCCTT , CM000666.1:g.155526080_155526083delinsCCTT	GRCh37
NC_000004.10:g.155745530_155745533delinsCCTT	NCBI36
NG_008834.1:g.12820_12823delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.1265_1268delinsAAGG MANE Select	ENSP00000336829.3:p.Glu422=
ENST00000336098.7:c.1265_1268delinsAAGG	ENSP00000336829.3:p.Glu422=
ENST00000404648.7:c.1265_1268delinsAAGG	ENSP00000384860.3:p.Glu422=
ENST00000405164.5:c.1289_1292delinsAAGG	ENSP00000384101.1:p.Glu430=
ENST00000407946.5:c.1289_1292delinsAAGG	ENSP00000384552.1:p.Glu430=
ENST00000465913.1:n.813_816delinsAAGG
ENST00000492082.5:n.1807_1810delinsAAGG
NM_000509.4:c.1265_1268delinsAAGG	NP_000500.2:p.Glu422=
NM_000509.5:c.1265_1268delinsAAGG	NP_000500.2:p.Glu422=
NM_021870.2:c.1265_1268delinsAAGG	NP_068656.2:p.Glu422=
NM_021870.3:c.1265_1268delinsAAGG MANE Select	NP_068656.2:p.Glu422=
NM_000509.6:c.1265_1268delinsAAGG	NP_000500.2:p.Glu422=