Canonical Allele Identifier: CA421930067

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169510251T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541013T>G , CM000663.2:g.169541013T>G	GRCh38
NC_000001.10:g.169510251T>G , CM000663.1:g.169510251T>G	GRCh37
NC_000001.9:g.167776875T>G	NCBI36
NG_011806.1:g.50519A>C , LRG_553:g.50519A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.4077A>C MANE Select	ENSP00000356771.3:p.Pro1359=
ENST00000367796.3:c.4092A>C	ENSP00000356770.3:p.Pro1364=
ENST00000367797.7:c.4077A>C	ENSP00000356771.3:p.Pro1359=
NM_000130.4:c.4077A>C , LRG_553t1:c.4077A>C	NP_000121.2:p.Pro1359=
XM_017000660.2:c.3666A>C	XP_016856149.1:p.Pro1222=
NM_000130.5:c.4077A>C MANE Select	NP_000121.2:p.Pro1359=