Canonical Allele Identifier: CA343128167
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552612T>C , CM000663.2:g.169552612T>C GRCh38
NC_000001.10:g.169521850T>C , CM000663.1:g.169521850T>C GRCh37
NC_000001.9:g.167788474T>C NCBI36
NG_011806.1:g.38920A>G , LRG_553:g.38920A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1241A>G MANE Select ENSP00000356771.3:p.Lys414Arg
ENST00000367796.3:c.1241A>G ENSP00000356770.3:p.Lys414Arg
ENST00000367797.7:c.1241A>G ENSP00000356771.3:p.Lys414Arg
NM_000130.4:c.1241A>G , LRG_553t1:c.1241A>G NP_000121.2:p.Lys414Arg
XM_017000660.2:c.830A>G XP_016856149.1:p.Lys277Arg
NM_000130.5:c.1241A>G MANE Select NP_000121.2:p.Lys414Arg