Canonical Allele Identifier: CA414920025

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154225320T>G (hg19) ; chrX:g.154997045T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997045T>G , CM000685.2:g.154997045T>G	GRCh38
NC_000023.10:g.154225320T>G , CM000685.1:g.154225320T>G	GRCh37
NC_000023.9:g.153878514T>G	NCBI36
NG_011403.1:g.30679A>C
NG_011403.2:g.30679A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.316A>C MANE Select	ENSP00000353393.4:p.Thr106Pro
ENST00000647125.1:c.*102A>C	ENSP00000496062.1:n.*102A>C
ENST00000360256.8:c.316A>C	ENSP00000353393.4:p.Thr106Pro
ENST00000423959.5:c.211A>C	ENSP00000409446.1:p.Thr71Pro
ENST00000453950.1:c.298A>C	ENSP00000389153.1:p.Thr100Pro
NM_000132.3:c.316A>C	NP_000123.1:p.Thr106Pro
XM_011531126.1:c.211A>C	XP_011529428.1:p.Thr71Pro
NM_000132.4:c.316A>C MANE Select	NP_000123.1:p.Thr106Pro