Canonical Allele Identifier: CA1229581991
Gene: FH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241511916A= , CM000663.2:g.241511916A= GRCh38
NC_000001.10:g.241675216A= , CM000663.1:g.241675216A= GRCh37
NC_000001.9:g.239741839A= NCBI36
NG_012338.1:g.12839T= , LRG_504:g.12839T=

Transcript Alleles

HGVS Amino-acid change
ENST00000493477.2:n.1058+51T=
ENST00000682162.1:c.584+51T= ENSP00000508203.1:n.584+51T=
ENST00000682567.1:n.632+51T=
ENST00000683521.1:c.555+51T= ENSP00000506864.1:n.555+51T=
ENST00000684483.1:c.555+51T= ENSP00000507894.1:n.555+51T=
ENST00000366560.4:c.555+51T= MANE Select ENSP00000355518.4:n.555+51T=
ENST00000366560.3:c.555+51T= ENSP00000355518.3:n.555+51T=
ENST00000497042.1:n.302T=
NM_000143.3:c.555+51T= , LRG_504t1:c.555+51T= NP_000134.2:n.555+51T=
XM_011544132.1:c.327+51T= XP_011542434.1:n.327+51T=
XM_011544132.2:c.327+51T= XP_011542434.1:n.327+51T=
NM_000143.4:c.555+51T= MANE Select NP_000134.2:n.555+51T=