Canonical Allele Identifier: CA2694838961

Gene: F9

Linked Data

• gnomAD v4: X-139536958-CATG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139536962_139536964del , CM000685.2:g.139536962_139536964del	GRCh38
NC_000023.10:g.138619121_138619123del , CM000685.1:g.138619121_138619123del	GRCh37
NC_000023.9:g.138446787_138446789del	NCBI36
NG_007994.1:g.11227_11229del , LRG_556:g.11227_11229del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.89-48_89-46del MANE Select	ENSP00000218099.2:n.89-48_89-46del
ENST00000218099.6:c.89-48_89-46del	ENSP00000218099.2:n.89-48_89-46del
ENST00000394090.2:c.89-48_89-46del	ENSP00000377650.2:n.89-48_89-46del
ENST00000479617.2:n.96-48_96-46del
NM_000133.3:c.89-48_89-46del , LRG_556t1:c.89-48_89-46del	NP_000124.1:n.89-48_89-46del
NM_001313913.1:c.89-48_89-46del	NP_001300842.1:n.89-48_89-46del
XM_005262397.3:c.89-48_89-46del	XP_005262454.1:n.89-48_89-46del
XM_005262397.4:c.89-48_89-46del	XP_005262454.1:n.89-48_89-46del
NM_000133.4:c.89-48_89-46del MANE Select	NP_000124.1:n.89-48_89-46del
NM_001313913.2:c.89-48_89-46del	NP_001300842.1:n.89-48_89-46del