Canonical Allele Identifier: CA414920052

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154225333A>T (hg19) ; chrX:g.154997058A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997058A>T , CM000685.2:g.154997058A>T	GRCh38
NC_000023.10:g.154225333A>T , CM000685.1:g.154225333A>T	GRCh37
NC_000023.9:g.153878527A>T	NCBI36
NG_011403.1:g.30666T>A
NG_011403.2:g.30666T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.303T>A MANE Select	ENSP00000353393.4:p.Asp101Glu
ENST00000647125.1:c.*89T>A	ENSP00000496062.1:n.*89T>A
ENST00000360256.8:c.303T>A	ENSP00000353393.4:p.Asp101Glu
ENST00000423959.5:c.198T>A	ENSP00000409446.1:p.Asp66Glu
ENST00000453950.1:c.285T>A	ENSP00000389153.1:p.Asp95Glu
NM_000132.3:c.303T>A	NP_000123.1:p.Asp101Glu
XM_011531126.1:c.198T>A	XP_011529428.1:p.Asp66Glu
NM_000132.4:c.303T>A MANE Select	NP_000123.1:p.Asp101Glu