Canonical Allele Identifier: CA2500458317
Gene: FH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241511766_241511767insTAGAGGACAGAGTGAAAAAGCAAGATGAAAGTTTTAA , CM000663.2:g.241511766_241511767insTAGAGGACAGAGTGAAAAAGCAAGATGAAAGTTTTAA GRCh38
NC_000001.10:g.241675066_241675067insTAGAGGACAGAGTGAAAAAGCAAGATGAAAGTTTTAA , CM000663.1:g.241675066_241675067insTAGAGGACAGAGTGAAAAAGCAAGATGAAAGTTTTAA GRCh37
NC_000001.9:g.239741689_239741690insTAGAGGACAGAGTGAAAAAGCAAGATGAAAGTTTTAA NCBI36
NG_012338.1:g.12988_12989insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA , LRG_504:g.12988_12989insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000493477.2:n.1058+200_1058+201insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA
ENST00000682162.1:c.584+200_584+201insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA ENSP00000508203.1:n.584+200_584+201insTTAAAACTTTCATCTTGCTTTTT...
ENST00000682567.1:n.632+200_632+201insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA
ENST00000683521.1:c.555+200_555+201insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA ENSP00000506864.1:n.555+200_555+201insTTAAAACTTTCATCTTGCTTTTT...
ENST00000684483.1:c.555+200_555+201insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA ENSP00000507894.1:n.555+200_555+201insTTAAAACTTTCATCTTGCTTTTT...
ENST00000366560.4:c.555+200_555+201insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA MANE Select ENSP00000355518.4:n.555+200_555+201insTTAAAACTTTCATCTTGCTTTTT...
ENST00000366560.3:c.555+200_555+201insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA ENSP00000355518.3:n.555+200_555+201insTTAAAACTTTCATCTTGCTTTTT...
NM_000143.3:c.555+200_555+201insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA , LRG_504t1:c.555+200_555+201insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA NP_000134.2:n.555+200_555+201insTTAAAACTTTCATCTTGCTTTTTCACTCT...
XM_011544132.1:c.327+200_327+201insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA XP_011542434.1:n.327+200_327+201insTTAAAACTTTCATCTTGCTTTTTCAC...
XM_011544132.2:c.327+200_327+201insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA XP_011542434.1:n.327+200_327+201insTTAAAACTTTCATCTTGCTTTTTCAC...
NM_000143.4:c.555+200_555+201insTTAAAACTTTCATCTTGCTTTTTCACTCTGTCCTCTA MANE Select NP_000134.2:n.555+200_555+201insTTAAAACTTTCATCTTGCTTTTTCACTCT...