Canonical Allele Identifier: CA343130771

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169498988G>C (hg19) ; chr1:g.169529750G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529750G>C , CM000663.2:g.169529750G>C	GRCh38
NC_000001.10:g.169498988G>C , CM000663.1:g.169498988G>C	GRCh37
NC_000001.9:g.167765612G>C	NCBI36
NG_011806.1:g.61782C>G , LRG_553:g.61782C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5277C>G MANE Select	ENSP00000356771.3:p.Asp1759Glu
ENST00000367796.3:c.5292C>G	ENSP00000356770.3:p.Asp1764Glu
ENST00000367797.7:c.5277C>G	ENSP00000356771.3:p.Asp1759Glu
NM_000130.4:c.5277C>G , LRG_553t1:c.5277C>G	NP_000121.2:p.Asp1759Glu
XM_017000660.2:c.4866C>G	XP_016856149.1:p.Asp1622Glu
NM_000130.5:c.5277C>G MANE Select	NP_000121.2:p.Asp1759Glu