Canonical Allele Identifier: CA1139667802

Gene: F9

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561569_139561580del , CM000685.2:g.139561569_139561580del	GRCh38
NC_000023.10:g.138643728_138643739del , CM000685.1:g.138643728_138643739del	GRCh37
NC_000023.9:g.138471394_138471405del	NCBI36
NG_007994.1:g.35834_35845del , LRG_556:g.35834_35845del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.884_895del MANE Select	ENSP00000218099.2:p.Asn295_Arg298del
ENST00000643157.1:n.1551_1562del
ENST00000218099.6:c.884_895del	ENSP00000218099.2:p.Asn295_Arg298del
ENST00000394090.2:c.770_781del	ENSP00000377650.2:p.Asn257_Arg260del
NM_000133.3:c.884_895del , LRG_556t1:c.884_895del	NP_000124.1:p.Asn295_Arg298del
NM_001313913.1:c.770_781del	NP_001300842.1:p.Asn257_Arg260del
XM_005262397.3:c.755_766del	XP_005262454.1:p.Asn252_Arg255del
XM_005262397.4:c.755_766del	XP_005262454.1:p.Asn252_Arg255del
NM_000133.4:c.884_895del MANE Select	NP_000124.1:p.Asn295_Arg298del
NM_001313913.2:c.770_781del	NP_001300842.1:p.Asn257_Arg260del