Canonical Allele Identifier: CA421930664

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169511043G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541805G>T , CM000663.2:g.169541805G>T	GRCh38
NC_000001.10:g.169511043G>T , CM000663.1:g.169511043G>T	GRCh37
NC_000001.9:g.167777667G>T	NCBI36
NG_011806.1:g.49727C>A , LRG_553:g.49727C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.3285C>A MANE Select	ENSP00000356771.3:p.Ala1095=
ENST00000367796.3:c.3300C>A	ENSP00000356770.3:p.Ala1100=
ENST00000367797.7:c.3285C>A	ENSP00000356771.3:p.Ala1095=
NM_000130.4:c.3285C>A , LRG_553t1:c.3285C>A	NP_000121.2:p.Ala1095=
XM_017000660.2:c.2874C>A	XP_016856149.1:p.Ala958=
NM_000130.5:c.3285C>A MANE Select	NP_000121.2:p.Ala1095=