Canonical Allele Identifier: CA414920096

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154225352A>T (hg19) ; chrX:g.154997077A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997077A>T , CM000685.2:g.154997077A>T	GRCh38
NC_000023.10:g.154225352A>T , CM000685.1:g.154225352A>T	GRCh37
NC_000023.9:g.153878546A>T	NCBI36
NG_011403.1:g.30647T>A
NG_011403.2:g.30647T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.284T>A MANE Select	ENSP00000353393.4:p.Ile95Asn
ENST00000647125.1:c.*70T>A	ENSP00000496062.1:n.*70T>A
ENST00000360256.8:c.284T>A	ENSP00000353393.4:p.Ile95Asn
ENST00000423959.5:c.179T>A	ENSP00000409446.1:p.Ile60Asn
ENST00000453950.1:c.266T>A	ENSP00000389153.1:p.Ile89Asn
NM_000132.3:c.284T>A	NP_000123.1:p.Ile95Asn
XM_011531126.1:c.179T>A	XP_011529428.1:p.Ile60Asn
NM_000132.4:c.284T>A MANE Select	NP_000123.1:p.Ile95Asn