Canonical Allele Identifier: CA2695237838

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896222_154896223insT , CM000685.2:g.154896222_154896223insT	GRCh38
NC_000023.10:g.154124497_154124498insT , CM000685.1:g.154124497_154124498insT	GRCh37
NC_000023.9:g.153777691_153777692insT	NCBI36
NG_011403.1:g.131501_131502insA
NG_011403.2:g.131501_131502insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6283_6284insA MANE Select	ENSP00000353393.4:p.Leu2095TyrfsTer?
ENST00000360256.8:c.6283_6284insA	ENSP00000353393.4:p.Leu2095TyrfsTer?
NM_000132.3:c.6283_6284insA	NP_000123.1:p.Leu2095TyrfsTer?
XM_011531126.1:c.6178_6179insA	XP_011529428.1:p.Leu2060TyrfsTer?
NM_000132.4:c.6283_6284insA MANE Select	NP_000123.1:p.Leu2095TyrfsTer?