Canonical Allele Identifier: CA1229580754

Gene: FH

Linked Data

• dbSNP Id: rs1660003224

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508893_241508894insTGAT , CM000663.2:g.241508893_241508894insTGAT	GRCh38
NC_000001.10:g.241672193_241672194insTGAT , CM000663.1:g.241672193_241672194insTGAT	GRCh37
NC_000001.9:g.239738816_239738817insTGAT	NCBI36
NG_012338.1:g.15861_15862insATCA , LRG_504:g.15861_15862insATCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1059-109_1059-108insATCA
ENST00000682162.1:c.585-109_585-108insATCA	ENSP00000508203.1:n.585-109_585-108insATCA
ENST00000682567.1:n.633-109_633-108insATCA
ENST00000683521.1:c.556-109_556-108insATCA	ENSP00000506864.1:n.556-109_556-108insATCA
ENST00000684161.1:n.1662_1663insATCA
ENST00000684483.1:c.556-134_556-133insATCA	ENSP00000507894.1:n.556-134_556-133insATCA
ENST00000366560.4:c.556-109_556-108insATCA MANE Select	ENSP00000355518.4:n.556-109_556-108insATCA
ENST00000366560.3:c.556-109_556-108insATCA	ENSP00000355518.3:n.556-109_556-108insATCA
NM_000143.3:c.556-109_556-108insATCA , LRG_504t1:c.556-109_556-108insATCA	NP_000134.2:n.556-109_556-108insATCA
XM_011544132.1:c.328-109_328-108insATCA	XP_011542434.1:n.328-109_328-108insATCA
XM_011544132.2:c.328-109_328-108insATCA	XP_011542434.1:n.328-109_328-108insATCA
NM_000143.4:c.556-109_556-108insATCA MANE Select	NP_000134.2:n.556-109_556-108insATCA