Canonical Allele Identifier: CA2579713822

Gene: F9

Linked Data

• gnomAD v4: X-139562149-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562152_139562153dup , CM000685.2:g.139562152_139562153dup	GRCh38
NC_000023.10:g.138644311_138644312dup , CM000685.1:g.138644311_138644312dup	GRCh37
NC_000023.9:g.138471977_138471978dup	NCBI36
NG_007994.1:g.36417_36418dup , LRG_556:g.36417_36418dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*81_*82dup MANE Select	ENSP00000218099.2:n.*81_*82dup
ENST00000643157.1:n.1723+411_1723+412dup
ENST00000218099.6:c.*81_*82dup	ENSP00000218099.2:n.*81_*82dup
NM_000133.3:c.*81_*82dup , LRG_556t1:c.*81_*82dup	NP_000124.1:n.*81_*82dup
NM_001313913.1:c.*81_*82dup	NP_001300842.1:n.*81_*82dup
XM_005262397.3:c.*81_*82dup	XP_005262454.1:n.*81_*82dup
XM_005262397.4:c.*81_*82dup	XP_005262454.1:n.*81_*82dup
NM_000133.4:c.*81_*82dup MANE Select	NP_000124.1:n.*81_*82dup
NM_001313913.2:c.*81_*82dup	NP_001300842.1:n.*81_*82dup