Canonical Allele Identifier: CA414915041

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154194365C>A (hg19) ; chrX:g.154966090C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154966090C>A , CM000685.2:g.154966090C>A	GRCh38
NC_000023.10:g.154194365C>A , CM000685.1:g.154194365C>A	GRCh37
NC_000023.9:g.153847559C>A	NCBI36
NG_011403.1:g.61634G>T
NG_011403.2:g.61634G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1323G>T MANE Select	ENSP00000353393.4:p.Lys441Asn
ENST00000647125.1:c.*1199G>T	ENSP00000496062.1:n.*1199G>T
ENST00000360256.8:c.1323G>T	ENSP00000353393.4:p.Lys441Asn
ENST00000483822.2:n.143G>T
NM_000132.3:c.1323G>T	NP_000123.1:p.Lys441Asn
XM_011531126.1:c.1218G>T	XP_011529428.1:p.Lys406Asn
NM_000132.4:c.1323G>T MANE Select	NP_000123.1:p.Lys441Asn