Canonical Allele Identifier: CA2365324117

Gene: SRSF6

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460723_43460735delinsGTCGATCACGTTC , CM000682.2:g.43460723_43460735delinsGTCGATCACGTTC	GRCh38
NC_000020.10:g.42089363_42089375delinsGTCGATCACGTTC , CM000682.1:g.42089363_42089375delinsGTCGATCACGTTC	GRCh37
NC_000020.9:g.41522777_41522789delinsGTCGATCACGTTC	NCBI36
NG_029906.1:g.7860_7872delinsGTCGATCACGTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.695_707delinsGTCGATCACGTTC MANE Select	ENSP00000244020.3:p.Gly232=
ENST00000657241.1:c.654+125_654+137delinsGTCGATCACGTTC
ENST00000662078.1:c.674+125_674+137delinsGTCGATCACGTTC	ENSP00000499666.1:n.674+125_674+137delinsGTCGATCACGTTC
ENST00000668808.1:c.695_707delinsGTCGATCACGTTC	ENSP00000499517.1:p.Gly232=
ENST00000670741.1:c.674+125_674+137delinsGTCGATCACGTTC	ENSP00000499492.1:n.674+125_674+137delinsGTCGATCACGTTC
ENST00000671022.1:n.785_797delinsGTCGATCACGTTC
ENST00000244020.4:c.695_707delinsGTCGATCACGTTC	ENSP00000244020.3:p.Gly232=
ENST00000483871.6:c.*555_*567delinsGTCGATCACGTTC	ENSP00000433544.1:n.*555_*567delinsGTCGATCACGTTC
NM_006275.5:c.695_707delinsGTCGATCACGTTC	NP_006266.2:p.Gly232=
NR_034009.1:n.1133_1145delinsGTCGATCACGTTC
XR_936608.1:n.1454_1466delinsGTCGATCACGTTC
XR_936608.2:n.1454_1466delinsGTCGATCACGTTC
NM_006275.6:c.695_707delinsGTCGATCACGTTC MANE Select	NP_006266.2:p.Gly232=
NR_034009.2:n.1101_1113delinsGTCGATCACGTTC