Canonical Allele Identifier: CA2365324145
Gene: SRSF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.43460789A= , CM000682.2:g.43460789A= GRCh38
NC_000020.10:g.42089429A= , CM000682.1:g.42089429A= GRCh37
NC_000020.9:g.41522843A= NCBI36
NG_029906.1:g.7926A=

Transcript Alleles

HGVS Amino-acid change
ENST00000244020.5:c.761A= MANE Select ENSP00000244020.3:p.Asp254=
ENST00000657241.1:c.654+191A=
ENST00000662078.1:c.674+191A= ENSP00000499666.1:n.674+191A=
ENST00000668808.1:c.761A= ENSP00000499517.1:p.Asp254=
ENST00000670741.1:c.674+191A= ENSP00000499492.1:n.674+191A=
ENST00000671022.1:n.851A=
ENST00000244020.4:c.761A= ENSP00000244020.3:p.Asp254=
ENST00000483871.6:c.*621A= ENSP00000433544.1:n.*621A=
NM_006275.5:c.761A= NP_006266.2:p.Asp254=
NR_034009.1:n.1199A=
XR_936608.1:n.1520A=
XR_936608.2:n.1520A=
NM_006275.6:c.761A= MANE Select NP_006266.2:p.Asp254=
NR_034009.2:n.1167A=