Canonical Allele Identifier: CA343118079

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169510925G>A (hg19) ; chr1:g.169541687G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541687G>A , CM000663.2:g.169541687G>A	GRCh38
NC_000001.10:g.169510925G>A , CM000663.1:g.169510925G>A	GRCh37
NC_000001.9:g.167777549G>A	NCBI36
NG_011806.1:g.49845C>T , LRG_553:g.49845C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3403C>T MANE Select	ENSP00000356771.3:p.Pro1135Ser
ENST00000367796.3:c.3418C>T	ENSP00000356770.3:p.Pro1140Ser
ENST00000367797.7:c.3403C>T	ENSP00000356771.3:p.Pro1135Ser
NM_000130.4:c.3403C>T , LRG_553t1:c.3403C>T	NP_000121.2:p.Pro1135Ser
XM_017000660.2:c.2992C>T	XP_016856149.1:p.Pro998Ser
NM_000130.5:c.3403C>T MANE Select	NP_000121.2:p.Pro1135Ser