Canonical Allele Identifier: CA1206140038
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541024_169541025delinsGC , CM000663.2:g.169541024_169541025delinsGC GRCh38
NC_000001.10:g.169510262_169510263delinsGC , CM000663.1:g.169510262_169510263delinsGC GRCh37
NC_000001.9:g.167776886_167776887delinsGC NCBI36
NG_011806.1:g.50507_50508delinsGC , LRG_553:g.50507_50508delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.4065_4066delinsGC MANE Select ENSP00000356771.3:p.Met1355=
ENST00000367796.3:c.4080_4081delinsGC ENSP00000356770.3:p.Met1360=
ENST00000367797.7:c.4065_4066delinsGC ENSP00000356771.3:p.Met1355=
NM_000130.4:c.4065_4066delinsGC , LRG_553t1:c.4065_4066delinsGC NP_000121.2:p.Met1355=
XM_017000660.2:c.3654_3655delinsGC XP_016856149.1:p.Met1218=
NM_000130.5:c.4065_4066delinsGC MANE Select NP_000121.2:p.Met1355=