Canonical Allele Identifier: CA2601806612

Gene: F9

Linked Data

• dbSNP Id: rs2148361082
• gnomAD v3: X-139548294-A-AAT
• gnomAD v4: X-139548294-A-AAT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548294_139548295insAT , CM000685.2:g.139548294_139548295insAT	GRCh38
NC_000023.10:g.138630453_138630454insAT , CM000685.1:g.138630453_138630454insAT	GRCh37
NC_000023.9:g.138458119_138458120insAT	NCBI36
NG_007994.1:g.22559_22560insAT , LRG_556:g.22559_22560insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-69_392-68insAT MANE Select	ENSP00000218099.2:n.392-69_392-68insAT
ENST00000643157.1:n.1059-69_1059-68insAT
ENST00000218099.6:c.392-69_392-68insAT	ENSP00000218099.2:n.392-69_392-68insAT
ENST00000394090.2:c.278-69_278-68insAT	ENSP00000377650.2:n.278-69_278-68insAT
ENST00000479617.2:n.345-69_345-68insAT
NM_000133.3:c.392-69_392-68insAT , LRG_556t1:c.392-69_392-68insAT	NP_000124.1:n.392-69_392-68insAT
NM_001313913.1:c.278-69_278-68insAT	NP_001300842.1:n.278-69_278-68insAT
XM_005262397.3:c.392-2768_392-2767insAT	XP_005262454.1:n.392-2768_392-2767insAT
XM_005262397.4:c.392-2768_392-2767insAT	XP_005262454.1:n.392-2768_392-2767insAT
NM_000133.4:c.392-69_392-68insAT MANE Select	NP_000124.1:n.392-69_392-68insAT
NM_001313913.2:c.278-69_278-68insAT	NP_001300842.1:n.278-69_278-68insAT