Canonical Allele Identifier: CA2695237427

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154969382_154969384del , CM000685.2:g.154969382_154969384del	GRCh38
NC_000023.10:g.154197657_154197659del , CM000685.1:g.154197657_154197659del	GRCh37
NC_000023.9:g.153850851_153850853del	NCBI36
NG_011403.1:g.58342_58344del
NG_011403.2:g.58342_58344del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.958_960del MANE Select	ENSP00000353393.4:p.Met320del
ENST00000647125.1:c.*834_*836del	ENSP00000496062.1:n.*834_*836del
ENST00000360256.8:c.958_960del	ENSP00000353393.4:p.Met320del
NM_000132.3:c.958_960del	NP_000123.1:p.Met320del
XM_011531126.1:c.853_855del	XP_011529428.1:p.Met285del
NM_000132.4:c.958_960del MANE Select	NP_000123.1:p.Met320del