Canonical Allele Identifier: CA343132137
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555305T>G , CM000663.2:g.169555305T>G GRCh38
NC_000001.10:g.169524543T>G , CM000663.1:g.169524543T>G GRCh37
NC_000001.9:g.167791167T>G NCBI36
NG_011806.1:g.36227A>C , LRG_553:g.36227A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.995A>C MANE Select ENSP00000356771.3:p.Lys332Thr
ENST00000367796.3:c.995A>C ENSP00000356770.3:p.Lys332Thr
ENST00000367797.7:c.995A>C ENSP00000356771.3:p.Lys332Thr
NM_000130.4:c.995A>C , LRG_553t1:c.995A>C NP_000121.2:p.Lys332Thr
XM_017000660.2:c.584A>C XP_016856149.1:p.Lys195Thr
NM_000130.5:c.995A>C MANE Select NP_000121.2:p.Lys332Thr