Canonical Allele Identifier: CA2461412164

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561756_139561758delinsAAG , CM000685.2:g.139561756_139561758delinsAAG	GRCh38
NC_000023.10:g.138643915_138643917delinsAAG , CM000685.1:g.138643915_138643917delinsAAG	GRCh37
NC_000023.9:g.138471581_138471583delinsAAG	NCBI36
NG_007994.1:g.36021_36023delinsAAG , LRG_556:g.36021_36023delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1071_1073delinsAAG MANE Select	ENSP00000218099.2:p.Gly357=
ENST00000643157.1:n.1723+15_1723+17delinsAAG
ENST00000218099.6:c.1071_1073delinsAAG	ENSP00000218099.2:p.Gly357=
ENST00000394090.2:c.957_959delinsAAG	ENSP00000377650.2:p.Gly319=
NM_000133.3:c.1071_1073delinsAAG , LRG_556t1:c.1071_1073delinsAAG	NP_000124.1:p.Gly357=
NM_001313913.1:c.957_959delinsAAG	NP_001300842.1:p.Gly319=
XM_005262397.3:c.942_944delinsAAG	XP_005262454.1:p.Gly314=
XM_005262397.4:c.942_944delinsAAG	XP_005262454.1:p.Gly314=
NM_000133.4:c.1071_1073delinsAAG MANE Select	NP_000124.1:p.Gly357=
NM_001313913.2:c.957_959delinsAAG	NP_001300842.1:p.Gly319=