Canonical Allele Identifier: CA2694839537

Gene: F9

Linked Data

• gnomAD v4: X-139548252-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548252_139548253insT , CM000685.2:g.139548252_139548253insT	GRCh38
NC_000023.10:g.138630411_138630412insT , CM000685.1:g.138630411_138630412insT	GRCh37
NC_000023.9:g.138458077_138458078insT	NCBI36
NG_007994.1:g.22517_22518insT , LRG_556:g.22517_22518insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-111_392-110insT MANE Select	ENSP00000218099.2:n.392-111_392-110insT
ENST00000643157.1:n.1059-111_1059-110insT
ENST00000218099.6:c.392-111_392-110insT	ENSP00000218099.2:n.392-111_392-110insT
ENST00000394090.2:c.278-111_278-110insT	ENSP00000377650.2:n.278-111_278-110insT
ENST00000479617.2:n.345-111_345-110insT
NM_000133.3:c.392-111_392-110insT , LRG_556t1:c.392-111_392-110insT	NP_000124.1:n.392-111_392-110insT
NM_001313913.1:c.278-111_278-110insT	NP_001300842.1:n.278-111_278-110insT
XM_005262397.3:c.392-2810_392-2809insT	XP_005262454.1:n.392-2810_392-2809insT
XM_005262397.4:c.392-2810_392-2809insT	XP_005262454.1:n.392-2810_392-2809insT
NM_000133.4:c.392-111_392-110insT MANE Select	NP_000124.1:n.392-111_392-110insT
NM_001313913.2:c.278-111_278-110insT	NP_001300842.1:n.278-111_278-110insT