Canonical Allele Identifier: CA2560679545

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860509_154860510insACATAAAAAGGTTGATATATGACCAAATTTT , CM000685.2:g.154860509_154860510insACATAAAAAGGTTGATATATGACCAAATTTT	GRCh38
NC_000023.10:g.154088784_154088785insACATAAAAAGGTTGATATATGACCAAATTTT , CM000685.1:g.154088784_154088785insACATAAAAAGGTTGATATATGACCAAATTTT	GRCh37
NC_000023.9:g.153741978_153741979insACATAAAAAGGTTGATATATGACCAAATTTT	NCBI36
NG_011403.1:g.167214_167215insAAAATTTGGTCATATATCAACCTTTTTATGT
NG_011403.2:g.167214_167215insAAAATTTGGTCATATATCAACCTTTTTATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6822_6823insAAAATTTGGTCATATATCAACCTTTTTATGT MANE Select	ENSP00000353393.4:p.Tyr2275LysfsTer?
ENST00000644698.1:c.555_556insAAAATTTGGTCATATATCAACCTTTTTATGT	ENSP00000495706.1:p.Tyr186LysfsTer?
ENST00000330287.10:c.417_418insAAAATTTGGTCATATATCAACCTTTTTATGT	ENSP00000327895.6:p.Tyr140LysfsTer?
ENST00000360256.8:c.6822_6823insAAAATTTGGTCATATATCAACCTTTTTATGT	ENSP00000353393.4:p.Tyr2275LysfsTer?
NM_000132.3:c.6822_6823insAAAATTTGGTCATATATCAACCTTTTTATGT	NP_000123.1:p.Tyr2275LysfsTer?
NM_019863.2:c.417_418insAAAATTTGGTCATATATCAACCTTTTTATGT	NP_063916.1:p.Tyr140LysfsTer?
XM_011531126.1:c.6717_6718insAAAATTTGGTCATATATCAACCTTTTTATGT	XP_011529428.1:p.Tyr2240LysfsTer?
NM_000132.4:c.6822_6823insAAAATTTGGTCATATATCAACCTTTTTATGT MANE Select	NP_000123.1:p.Tyr2275LysfsTer?
NM_019863.3:c.417_418insAAAATTTGGTCATATATCAACCTTTTTATGT	NP_063916.1:p.Tyr140LysfsTer?