Canonical Allele Identifier: CA645528099

Gene: F5

Linked Data

• COSMIC: COSM5702460

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169555193_169555194delinsTT , CM000663.2:g.169555193_169555194delinsTT	GRCh38
NC_000001.10:g.169524431_169524432delinsTT , CM000663.1:g.169524431_169524432delinsTT	GRCh37
NC_000001.9:g.167791055_167791056delinsTT	NCBI36
NG_011806.1:g.36338_36339delinsAA , LRG_553:g.36338_36339delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1106_1107delinsAA MANE Select	ENSP00000356771.3:p.Ala369Glu
ENST00000367796.3:c.1106_1107delinsAA	ENSP00000356770.3:p.Ala369Glu
ENST00000367797.7:c.1106_1107delinsAA	ENSP00000356771.3:p.Ala369Glu
NM_000130.4:c.1106_1107delinsAA , LRG_553t1:c.1106_1107delinsAA	NP_000121.2:p.Ala369Glu
XM_017000660.2:c.695_696delinsAA	XP_016856149.1:p.Ala232Glu
NM_000130.5:c.1106_1107delinsAA MANE Select	NP_000121.2:p.Ala369Glu