Canonical Allele Identifier: CA10529787

Gene: F9

Linked Data

• dbSNP Id: rs774673930
• ExAC: X:138630471 TTAGAA / T
• gnomAD v2: X-138630471-TTAGAA-T
• gnomAD v3: X-139548312-TTAGAA-T
• gnomAD v4: X-139548312-TTAGAA-T
• MyVariant Identifiers: chrX:g.138630472_138630476del (hg19) ; chrX:g.139548313_139548317del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548313_139548317del , CM000685.2:g.139548313_139548317del	GRCh38
NC_000023.10:g.138630472_138630476del , CM000685.1:g.138630472_138630476del	GRCh37
NC_000023.9:g.138458138_138458142del	NCBI36
NG_007994.1:g.22578_22582del , LRG_556:g.22578_22582del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-50_392-46del MANE Select	ENSP00000218099.2:n.392-50_392-46del
ENST00000643157.1:n.1059-50_1059-46del
ENST00000218099.6:c.392-50_392-46del	ENSP00000218099.2:n.392-50_392-46del
ENST00000394090.2:c.278-50_278-46del	ENSP00000377650.2:n.278-50_278-46del
ENST00000479617.2:n.345-50_345-46del
NM_000133.3:c.392-50_392-46del , LRG_556t1:c.392-50_392-46del	NP_000124.1:n.392-50_392-46del
NM_001313913.1:c.278-50_278-46del	NP_001300842.1:n.278-50_278-46del
XM_005262397.3:c.392-2749_392-2745del	XP_005262454.1:n.392-2749_392-2745del
XM_005262397.4:c.392-2749_392-2745del	XP_005262454.1:n.392-2749_392-2745del
NM_000133.4:c.392-50_392-46del MANE Select	NP_000124.1:n.392-50_392-46del
NM_001313913.2:c.278-50_278-46del	NP_001300842.1:n.278-50_278-46del