Canonical Allele Identifier: CA10608168

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169524904A>G , CM000663.2:g.169524904A>G	GRCh38
NC_000001.10:g.169494142A>G , CM000663.1:g.169494142A>G	GRCh37
NC_000001.9:g.167760766A>G	NCBI36
NG_011806.1:g.66628T>C , LRG_553:g.66628T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000130.5:c.5721T>C MANE Select	NP_000121.2:p.Cys1907=
ENST00000367797.9:c.5721T>C MANE Select	ENSP00000356771.3:p.Cys1907=
NM_000130.4:c.5721T>C , LRG_553t1:c.5721T>C	NP_000121.2:p.Cys1907=
ENST00000367796.3:c.5736T>C	ENSP00000356770.3:p.Cys1912=
ENST00000367797.7:c.5721T>C	ENSP00000356771.3:p.Cys1907=
XM_017000660.2:c.5310T>C	XP_016856149.1:p.Cys1770=