Canonical Allele Identifier: CA2365324148
Gene: SRSF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.43460794G= , CM000682.2:g.43460794G= GRCh38
NC_000020.10:g.42089434G= , CM000682.1:g.42089434G= GRCh37
NC_000020.9:g.41522848G= NCBI36
NG_029906.1:g.7931G=

Transcript Alleles

HGVS Amino-acid change
ENST00000244020.5:c.766G= MANE Select ENSP00000244020.3:p.Gly256=
ENST00000657241.1:c.654+196G=
ENST00000662078.1:c.674+196G= ENSP00000499666.1:n.674+196G=
ENST00000668808.1:c.766G= ENSP00000499517.1:p.Gly256=
ENST00000670741.1:c.674+196G= ENSP00000499492.1:n.674+196G=
ENST00000671022.1:n.856G=
ENST00000244020.4:c.766G= ENSP00000244020.3:p.Gly256=
ENST00000483871.6:c.*626G= ENSP00000433544.1:n.*626G=
NM_006275.5:c.766G= NP_006266.2:p.Gly256=
NR_034009.1:n.1204G=
XR_936608.1:n.1525G=
XR_936608.2:n.1525G=
NM_006275.6:c.766G= MANE Select NP_006266.2:p.Gly256=
NR_034009.2:n.1172G=