Canonical Allele Identifier: CA421738229

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169541505G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572267G>T , CM000663.2:g.169572267G>T	GRCh38
NC_000001.10:g.169541505G>T , CM000663.1:g.169541505G>T	GRCh37
NC_000001.9:g.167808129G>T	NCBI36
NG_011806.1:g.19265C>A , LRG_553:g.19265C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.327C>A MANE Select	ENSP00000356771.3:p.Pro109=
ENST00000367796.3:c.327C>A	ENSP00000356770.3:p.Pro109=
ENST00000367797.7:c.327C>A	ENSP00000356771.3:p.Pro109=
NM_000130.4:c.327C>A , LRG_553t1:c.327C>A	NP_000121.2:p.Pro109=
XM_017000660.2:c.-85C>A	XP_016856149.1:n.-85C>A
NM_000130.5:c.327C>A MANE Select	NP_000121.2:p.Pro109=