Canonical Allele Identifier: CA1141934523
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555304T= , CM000663.2:g.169555304T= GRCh38
NC_000001.10:g.169524542T= , CM000663.1:g.169524542T= GRCh37
NC_000001.9:g.167791166T= NCBI36
NG_011806.1:g.36228A= , LRG_553:g.36228A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.996A= MANE Select ENSP00000356771.3:p.Lys332=
ENST00000367796.3:c.996A= ENSP00000356770.3:p.Lys332=
ENST00000367797.7:c.996A= ENSP00000356771.3:p.Lys332=
NM_000130.4:c.996A= , LRG_553t1:c.996A= NP_000121.2:p.Lys332=
XM_017000660.2:c.585A= XP_016856149.1:p.Lys195=
NM_000130.5:c.996A= MANE Select NP_000121.2:p.Lys332=