Canonical Allele Identifier: CA414919891

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154225260T>A (hg19) ; chrX:g.154996985T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154996985T>A , CM000685.2:g.154996985T>A	GRCh38
NC_000023.10:g.154225260T>A , CM000685.1:g.154225260T>A	GRCh37
NC_000023.9:g.153878454T>A	NCBI36
NG_011403.1:g.30739A>T
NG_011403.2:g.30739A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.376A>T MANE Select	ENSP00000353393.4:p.Lys126Ter
ENST00000647125.1:c.*162A>T	ENSP00000496062.1:n.*162A>T
ENST00000360256.8:c.376A>T	ENSP00000353393.4:p.Lys126Ter
ENST00000423959.5:c.271A>T	ENSP00000409446.1:p.Lys91Ter
ENST00000453950.1:c.358A>T	ENSP00000389153.1:p.Lys120Ter
NM_000132.3:c.376A>T	NP_000123.1:p.Lys126Ter
XM_011531126.1:c.271A>T	XP_011529428.1:p.Lys91Ter
NM_000132.4:c.376A>T MANE Select	NP_000123.1:p.Lys126Ter