Canonical Allele Identifier: CA913410872

Gene: FH

Linked Data

• gnomAD v2: 1-241665873-T-TGATG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502573_241502574insGATG , CM000663.2:g.241502573_241502574insGATG	GRCh38
NC_000001.10:g.241665873_241665874insGATG , CM000663.1:g.241665873_241665874insGATG	GRCh37
NC_000001.9:g.239732496_239732497insGATG	NCBI36
NG_012338.1:g.22181_22182insCATC , LRG_504:g.22181_22182insCATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1612-4_1612-3insCATC
ENST00000682162.1:c.1138-4_1138-3insCATC	ENSP00000508203.1:n.1138-4_1138-3insCATC
ENST00000682567.1:n.2653_2654insCATC
ENST00000683521.1:c.1109-4_1109-3insCATC	ENSP00000506864.1:n.1109-4_1109-3insCATC
ENST00000684161.1:n.2324-4_2324-3insCATC
ENST00000684483.1:c.*505-4_*505-3insCATC	ENSP00000507894.1:n.*505-4_*505-3insCATC
ENST00000366560.4:c.1109-4_1109-3insCATC MANE Select	ENSP00000355518.4:n.1109-4_1109-3insCATC
ENST00000366560.3:c.1109-4_1109-3insCATC	ENSP00000355518.3:n.1109-4_1109-3insCATC
NM_000143.3:c.1109-4_1109-3insCATC , LRG_504t1:c.1109-4_1109-3insCATC	NP_000134.2:n.1109-4_1109-3insCATC
XM_011544132.1:c.881-4_881-3insCATC	XP_011542434.1:n.881-4_881-3insCATC
XM_011544132.2:c.881-4_881-3insCATC	XP_011542434.1:n.881-4_881-3insCATC
NM_000143.4:c.1109-4_1109-3insCATC MANE Select	NP_000134.2:n.1109-4_1109-3insCATC