Canonical Allele Identifier: CA2651255174

Gene: FH

Linked Data

• gnomAD v4: 1-241511796-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241511798del , CM000663.2:g.241511798del	GRCh38
NC_000001.10:g.241675098del , CM000663.1:g.241675098del	GRCh37
NC_000001.9:g.239741721del	NCBI36
NG_012338.1:g.12958del , LRG_504:g.12958del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1058+170del
ENST00000682162.1:c.584+170del	ENSP00000508203.1:n.584+170del
ENST00000682567.1:n.632+170del
ENST00000683521.1:c.555+170del	ENSP00000506864.1:n.555+170del
ENST00000684483.1:c.555+170del	ENSP00000507894.1:n.555+170del
ENST00000366560.4:c.555+170del MANE Select	ENSP00000355518.4:n.555+170del
ENST00000366560.3:c.555+170del	ENSP00000355518.3:n.555+170del
NM_000143.3:c.555+170del , LRG_504t1:c.555+170del	NP_000134.2:n.555+170del
XM_011544132.1:c.327+170del	XP_011542434.1:n.327+170del
XM_011544132.2:c.327+170del	XP_011542434.1:n.327+170del
NM_000143.4:c.555+170del MANE Select	NP_000134.2:n.555+170del