Canonical Allele Identifier: CA2365324031
Gene: SRSF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.43460570T= , CM000682.2:g.43460570T= GRCh38
NC_000020.10:g.42089210T= , CM000682.1:g.42089210T= GRCh37
NC_000020.9:g.41522624T= NCBI36
NG_029906.1:g.7707T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000244020.5:c.646T= MANE Select ENSP00000244020.3:p.Ser216=
ENST00000657241.1:c.626T=
ENST00000662078.1:c.646T= ENSP00000499666.1:p.Ser216=
ENST00000668808.1:c.646T= ENSP00000499517.1:p.Ser216=
ENST00000670741.1:c.646T= ENSP00000499492.1:p.Ser216=
ENST00000671022.1:n.736T=
ENST00000244020.4:c.646T= ENSP00000244020.3:p.Ser216=
ENST00000483871.6:c.*506T= ENSP00000433544.1:n.*506T=
NM_006275.5:c.646T= NP_006266.2:p.Ser216=
NR_034009.1:n.1084T=
XR_936608.1:n.1405T=
XR_936608.2:n.1405T=
NM_006275.6:c.646T= MANE Select NP_006266.2:p.Ser216=
NR_034009.2:n.1052T=