Canonical Allele Identifier: CA336142645

Gene: F9

Linked Data

• dbSNP Id: rs963171779
• gnomAD v3: X-139560916-AC-A
• gnomAD v4: X-139560916-AC-A
• MyVariant Identifiers: chrX:g.138643076del (hg19) ; chrX:g.139560917del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560918del , CM000685.2:g.139560918del	GRCh38
NC_000023.10:g.138643077del , CM000685.1:g.138643077del	GRCh37
NC_000023.9:g.138470743del	NCBI36
NG_007994.1:g.35183del , LRG_556:g.35183del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.838+63del MANE Select	ENSP00000218099.2:n.838+63del
ENST00000643157.1:n.1505+63del
ENST00000218099.6:c.838+63del	ENSP00000218099.2:n.838+63del
ENST00000394090.2:c.724+63del	ENSP00000377650.2:n.724+63del
NM_000133.3:c.838+63del , LRG_556t1:c.838+63del	NP_000124.1:n.838+63del
NM_001313913.1:c.724+63del	NP_001300842.1:n.724+63del
XM_005262397.3:c.709+63del	XP_005262454.1:n.709+63del
XM_005262397.4:c.709+63del	XP_005262454.1:n.709+63del
NM_000133.4:c.838+63del MANE Select	NP_000124.1:n.838+63del
NM_001313913.2:c.724+63del	NP_001300842.1:n.724+63del