Canonical Allele Identifier: CA2695238478

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154996997delinsAA , CM000685.2:g.154996997delinsAA	GRCh38
NC_000023.10:g.154225272delinsAA , CM000685.1:g.154225272delinsAA	GRCh37
NC_000023.9:g.153878466delinsAA	NCBI36
NG_011403.1:g.30727delinsTT
NG_011403.2:g.30727delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.364delinsTT MANE Select	ENSP00000353393.4:p.Val122PhefsTer8
ENST00000647125.1:c.*150delinsTT	ENSP00000496062.1:n.*150delinsTT
ENST00000360256.8:c.364delinsTT	ENSP00000353393.4:p.Val122PhefsTer8
ENST00000423959.5:c.259delinsTT	ENSP00000409446.1:p.Val87PhefsTer8
ENST00000453950.1:c.346delinsTT	ENSP00000389153.1:p.Val116PhefsTer8
NM_000132.3:c.364delinsTT	NP_000123.1:p.Val122PhefsTer8
XM_011531126.1:c.259delinsTT	XP_011529428.1:p.Val87PhefsTer8
NM_000132.4:c.364delinsTT MANE Select	NP_000123.1:p.Val122PhefsTer8