Canonical Allele Identifier: CA1234730

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169586232G>C , CM000663.2:g.169586232G>C	GRCh38
NC_000001.10:g.169555470G>C , CM000663.1:g.169555470G>C	GRCh37
NC_000001.9:g.167822094G>C	NCBI36
NG_011806.1:g.5300C>G , LRG_553:g.5300C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000130.5:c.155C>G MANE Select	NP_000121.2:p.Ser52Ter
ENST00000367797.9:c.155C>G MANE Select	ENSP00000356771.3:p.Ser52Ter
NM_000130.4:c.155C>G , LRG_553t1:c.155C>G	NP_000121.2:p.Ser52Ter
ENST00000367796.3:c.155C>G	ENSP00000356770.3:p.Ser52Ter
ENST00000367797.7:c.155C>G	ENSP00000356771.3:p.Ser52Ter
XM_017000660.2:c.-165C>G	XP_016856149.1:n.-165C>G