Canonical Allele Identifier: CA2695238528
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022454_155022458delinsACTTTGCAT , CM000685.2:g.155022454_155022458delinsACTTTGCAT GRCh38
NC_000023.10:g.154250729_154250733delinsACTTTGCAT , CM000685.1:g.154250729_154250733delinsACTTTGCAT GRCh37
NC_000023.9:g.153903923_153903927delinsACTTTGCAT NCBI36
NG_011403.1:g.5266_5270delinsATGCAAAGT
NG_011403.2:g.5266_5270delinsATGCAAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.95_99delinsATGCAAAGT MANE Select ENSP00000353393.4:p.Ser32TyrfsTer4
ENST00000647125.1:c.95_99delinsATGCAAAGT ENSP00000496062.1:p.Ser32TyrfsTer4
ENST00000360256.8:c.95_99delinsATGCAAAGT ENSP00000353393.4:p.Ser32TyrfsTer4
ENST00000423959.5:c.38+4322_38+4326delinsATGCAAAGT ENSP00000409446.1:n.38+4322_38+4326delinsATGCAAAGT
ENST00000453950.1:c.77_81delinsATGCAAAGT ENSP00000389153.1:p.Ser26TyrfsTer4
NM_000132.3:c.95_99delinsATGCAAAGT NP_000123.1:p.Ser32TyrfsTer4
XM_011531126.1:c.38+4322_38+4326delinsATGCAAAGT XP_011529428.1:n.38+4322_38+4326delinsATGCAAAGT
NM_000132.4:c.95_99delinsATGCAAAGT MANE Select NP_000123.1:p.Ser32TyrfsTer4