Canonical Allele Identifier: CA414896712

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154065900A>G (hg19) ; chrX:g.154837625A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837625A>G , CM000685.2:g.154837625A>G	GRCh38
NC_000023.10:g.154065900A>G , CM000685.1:g.154065900A>G	GRCh37
NC_000023.9:g.153719094A>G	NCBI36
NG_011403.1:g.190099T>C
NG_033065.1:g.2038T>C
NG_011403.2:g.190099T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.7028T>C MANE Select	ENSP00000353393.4:p.Leu2343Pro
ENST00000644698.1:c.761T>C	ENSP00000495706.1:p.Leu254Pro
ENST00000330287.10:c.623T>C	ENSP00000327895.6:p.Leu208Pro
ENST00000360256.8:c.7028T>C	ENSP00000353393.4:p.Leu2343Pro
NM_000132.3:c.7028T>C	NP_000123.1:p.Leu2343Pro
NM_019863.2:c.623T>C	NP_063916.1:p.Leu208Pro
XM_011531126.1:c.6923T>C	XP_011529428.1:p.Leu2308Pro
NM_000132.4:c.7028T>C MANE Select	NP_000123.1:p.Leu2343Pro
NM_019863.3:c.623T>C	NP_063916.1:p.Leu208Pro