Canonical Allele Identifier: CA1229580608
Gene: FH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241508599_241508619delinsATACCTGCCCAAGAGTAAGTG , CM000663.2:g.241508599_241508619delinsATACCTGCCCAAGAGTAAGTG GRCh38
NC_000001.10:g.241671899_241671919delinsATACCTGCCCAAGAGTAAGTG , CM000663.1:g.241671899_241671919delinsATACCTGCCCAAGAGTAAGTG GRCh37
NC_000001.9:g.239738522_239738542delinsATACCTGCCCAAGAGTAAGTG NCBI36
NG_012338.1:g.16136_16156delinsCACTTACTCTTGGGCAGGTAT , LRG_504:g.16136_16156delinsCACTTACTCTTGGGCAGGTAT

Transcript Alleles

HGVS Amino-acid change
ENST00000493477.2:n.1225_1241+4delinsCACTTACTCTTGGGCAGGTAT
ENST00000682162.1:c.751_767+4delinsCACTTACTCTTGGGCAGGTAT
ENST00000682567.1:n.799_815+4delinsCACTTACTCTTGGGCAGGTAT
ENST00000683521.1:c.722_738+4delinsCACTTACTCTTGGGCAGGTAT
ENST00000684161.1:n.1937_1953+4delinsCACTTACTCTTGGGCAGGTAT
ENST00000684483.1:c.*118_*134+4delinsCACTTACTCTTGGGCAGGTAT
ENST00000366560.4:c.722_738+4delinsCACTTACTCTTGGGCAGGTAT
ENST00000366560.3:c.722_738+4delinsCACTTACTCTTGGGCAGGTAT
NM_000143.3:c.722_738+4delinsCACTTACTCTTGGGCAGGTAT , LRG_504t1:c.722_738+4delinsCACTTACTCTTGGGCAGGTAT
XM_011544132.1:c.494_510+4delinsCACTTACTCTTGGGCAGGTAT
XM_011544132.2:c.494_510+4delinsCACTTACTCTTGGGCAGGTAT
NM_000143.4:c.722_738+4delinsCACTTACTCTTGGGCAGGTAT