Canonical Allele Identifier: CA645610452

Gene: F9

Linked Data

• COSMIC: COSM5802083

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551129dup , CM000685.2:g.139551129dup	GRCh38
NC_000023.10:g.138633288dup , CM000685.1:g.138633288dup	GRCh37
NC_000023.9:g.138460954dup	NCBI36
NG_007994.1:g.25394dup , LRG_556:g.25394dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.588dup MANE Select	ENSP00000218099.2:p.Pro197SerfsTer2
ENST00000643157.1:n.1255dup
ENST00000218099.6:c.588dup	ENSP00000218099.2:p.Pro197SerfsTer2
ENST00000394090.2:c.474dup	ENSP00000377650.2:p.Pro159SerfsTer2
NM_000133.3:c.588dup , LRG_556t1:c.588dup	NP_000124.1:p.Pro197SerfsTer2
NM_001313913.1:c.474dup	NP_001300842.1:p.Pro159SerfsTer2
XM_005262397.3:c.459dup	XP_005262454.1:p.Pro154SerfsTer2
XM_005262397.4:c.459dup	XP_005262454.1:p.Pro154SerfsTer2
NM_000133.4:c.588dup MANE Select	NP_000124.1:p.Pro197SerfsTer2
NM_001313913.2:c.474dup	NP_001300842.1:p.Pro159SerfsTer2