Canonical Allele Identifier: CA343118008
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541677A>T , CM000663.2:g.169541677A>T GRCh38
NC_000001.10:g.169510915A>T , CM000663.1:g.169510915A>T GRCh37
NC_000001.9:g.167777539A>T NCBI36
NG_011806.1:g.49855T>A , LRG_553:g.49855T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.3413T>A MANE Select ENSP00000356771.3:p.Met1138Lys
ENST00000367796.3:c.3428T>A ENSP00000356770.3:p.Met1143Lys
ENST00000367797.7:c.3413T>A ENSP00000356771.3:p.Met1138Lys
NM_000130.4:c.3413T>A , LRG_553t1:c.3413T>A NP_000121.2:p.Met1138Lys
XM_017000660.2:c.3002T>A XP_016856149.1:p.Met1001Lys
NM_000130.5:c.3413T>A MANE Select NP_000121.2:p.Met1138Lys