Canonical Allele Identifier: CA421734061

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169524584A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555346A>T , CM000663.2:g.169555346A>T	GRCh38
NC_000001.10:g.169524584A>T , CM000663.1:g.169524584A>T	GRCh37
NC_000001.9:g.167791208A>T	NCBI36
NG_011806.1:g.36186T>A , LRG_553:g.36186T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.954T>A MANE Select	ENSP00000356771.3:p.Ala318=
ENST00000367796.3:c.954T>A	ENSP00000356770.3:p.Ala318=
ENST00000367797.7:c.954T>A	ENSP00000356771.3:p.Ala318=
NM_000130.4:c.954T>A , LRG_553t1:c.954T>A	NP_000121.2:p.Ala318=
XM_017000660.2:c.543T>A	XP_016856149.1:p.Ala181=
NM_000130.5:c.954T>A MANE Select	NP_000121.2:p.Ala318=