Canonical Allele Identifier: CA343123533

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169523900G>C , CM000663.2:g.169523900G>C	GRCh38
NC_000001.10:g.169493138G>C , CM000663.1:g.169493138G>C	GRCh37
NC_000001.9:g.167759762G>C	NCBI36
NG_011806.1:g.67632C>G , LRG_553:g.67632C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000130.5:c.5793C>G MANE Select	NP_000121.2:p.Tyr1931Ter
ENST00000367797.9:c.5793C>G MANE Select	ENSP00000356771.3:p.Tyr1931Ter
NM_000130.4:c.5793C>G , LRG_553t1:c.5793C>G	NP_000121.2:p.Tyr1931Ter
ENST00000367796.3:c.5808C>G	ENSP00000356770.3:p.Tyr1936Ter
ENST00000367797.7:c.5793C>G	ENSP00000356771.3:p.Tyr1931Ter
XM_017000660.2:c.5382C>G	XP_016856149.1:p.Tyr1794Ter