Canonical Allele Identifier: CA409071543
Gene: SRSF6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.43460784G>T , CM000682.2:g.43460784G>T GRCh38
NC_000020.10:g.42089424G>T , CM000682.1:g.42089424G>T GRCh37
NC_000020.9:g.41522838G>T NCBI36
NG_029906.1:g.7921G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000244020.5:c.756G>T MANE Select ENSP00000244020.3:p.Lys252Asn
ENST00000657241.1:c.654+186G>T
ENST00000662078.1:c.674+186G>T ENSP00000499666.1:n.674+186G>T
ENST00000668808.1:c.756G>T ENSP00000499517.1:p.Lys252Asn
ENST00000670741.1:c.674+186G>T ENSP00000499492.1:n.674+186G>T
ENST00000671022.1:n.846G>T
ENST00000244020.4:c.756G>T ENSP00000244020.3:p.Lys252Asn
ENST00000483871.6:c.*616G>T ENSP00000433544.1:n.*616G>T
NM_006275.5:c.756G>T NP_006266.2:p.Lys252Asn
NR_034009.1:n.1194G>T
XR_936608.1:n.1515G>T
XR_936608.2:n.1515G>T
NM_006275.6:c.756G>T MANE Select NP_006266.2:p.Lys252Asn
NR_034009.2:n.1162G>T