Canonical Allele Identifier: CA2695236351

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561815_139561817del , CM000685.2:g.139561815_139561817del	GRCh38
NC_000023.10:g.138643974_138643976del , CM000685.1:g.138643974_138643976del	GRCh37
NC_000023.9:g.138471640_138471642del	NCBI36
NG_007994.1:g.36080_36082del , LRG_556:g.36080_36082del

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.1130_1132del MANE Select	ENSP00000218099.2:p.Val377del
ENST00000643157.1:n.1723+74_1723+76del
ENST00000218099.6:c.1130_1132del	ENSP00000218099.2:p.Val377del
ENST00000394090.2:c.1016_1018del	ENSP00000377650.2:p.Val339del
NM_000133.3:c.1130_1132del , LRG_556t1:c.1130_1132del	NP_000124.1:p.Val377del
NM_001313913.1:c.1016_1018del	NP_001300842.1:p.Val339del
XM_005262397.3:c.1001_1003del	XP_005262454.1:p.Val334del
XM_005262397.4:c.1001_1003del	XP_005262454.1:p.Val334del
NM_000133.4:c.1130_1132del MANE Select	NP_000124.1:p.Val377del
NM_001313913.2:c.1016_1018del	NP_001300842.1:p.Val339del