Canonical Allele Identifier: CA2573159300

Gene: F9

Linked Data

• ClinVar Variation Id: 1640487
• ClinVar RCV Id: RCV002139883
• dbSNP Id: rs2148353026

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139530862_139530863del , CM000685.2:g.139530862_139530863del	GRCh38
NC_000023.10:g.138613021_138613022del , CM000685.1:g.138613021_138613022del	GRCh37
NC_000023.9:g.138440687_138440688del	NCBI36
NG_007994.1:g.5127_5128del , LRG_556:g.5127_5128del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.88+10_88+11del MANE Select	ENSP00000218099.2:n.88+10_88+11del
ENST00000218099.6:c.88+10_88+11del	ENSP00000218099.2:n.88+10_88+11del
ENST00000394090.2:c.88+10_88+11del	ENSP00000377650.2:n.88+10_88+11del
ENST00000479617.2:n.95+10_95+11del
NM_000133.3:c.88+10_88+11del , LRG_556t1:c.88+10_88+11del	NP_000124.1:n.88+10_88+11del
NM_001313913.1:c.88+10_88+11del	NP_001300842.1:n.88+10_88+11del
XM_005262397.3:c.88+10_88+11del	XP_005262454.1:n.88+10_88+11del
XM_005262397.4:c.88+10_88+11del	XP_005262454.1:n.88+10_88+11del
NM_000133.4:c.88+10_88+11del MANE Select	NP_000124.1:n.88+10_88+11del
NM_001313913.2:c.88+10_88+11del	NP_001300842.1:n.88+10_88+11del