Canonical Allele Identifier: CA414919890

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154225259T>G (hg19) ; chrX:g.154996984T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154996984T>G , CM000685.2:g.154996984T>G	GRCh38
NC_000023.10:g.154225259T>G , CM000685.1:g.154225259T>G	GRCh37
NC_000023.9:g.153878453T>G	NCBI36
NG_011403.1:g.30740A>C
NG_011403.2:g.30740A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.377A>C MANE Select	ENSP00000353393.4:p.Lys126Thr
ENST00000647125.1:c.*163A>C	ENSP00000496062.1:n.*163A>C
ENST00000360256.8:c.377A>C	ENSP00000353393.4:p.Lys126Thr
ENST00000423959.5:c.272A>C	ENSP00000409446.1:p.Lys91Thr
ENST00000453950.1:c.359A>C	ENSP00000389153.1:p.Lys120Thr
NM_000132.3:c.377A>C	NP_000123.1:p.Lys126Thr
XM_011531126.1:c.272A>C	XP_011529428.1:p.Lys91Thr
NM_000132.4:c.377A>C MANE Select	NP_000123.1:p.Lys126Thr