Canonical Allele Identifier: CA343130701

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169498984T>A (hg19) ; chr1:g.169529746T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529746T>A , CM000663.2:g.169529746T>A	GRCh38
NC_000001.10:g.169498984T>A , CM000663.1:g.169498984T>A	GRCh37
NC_000001.9:g.167765608T>A	NCBI36
NG_011806.1:g.61786A>T , LRG_553:g.61786A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5281A>T MANE Select	ENSP00000356771.3:p.Asn1761Tyr
ENST00000367796.3:c.5296A>T	ENSP00000356770.3:p.Asn1766Tyr
ENST00000367797.7:c.5281A>T	ENSP00000356771.3:p.Asn1761Tyr
NM_000130.4:c.5281A>T , LRG_553t1:c.5281A>T	NP_000121.2:p.Asn1761Tyr
XM_017000660.2:c.4870A>T	XP_016856149.1:p.Asn1624Tyr
NM_000130.5:c.5281A>T MANE Select	NP_000121.2:p.Asn1761Tyr