Canonical Allele Identifier: CA510737306

Gene: SRSF6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460871T>A , CM000682.2:g.43460871T>A	GRCh38
NC_000020.10:g.42089511T>A , CM000682.1:g.42089511T>A	GRCh37
NC_000020.9:g.41522925T>A	NCBI36
NG_029906.1:g.8008T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.843T>A MANE Select	ENSP00000244020.3:p.Pro281=
ENST00000657241.1:c.654+273T>A
ENST00000662078.1:c.674+273T>A	ENSP00000499666.1:n.674+273T>A
ENST00000668808.1:c.824+19T>A	ENSP00000499517.1:n.824+19T>A
ENST00000670741.1:c.674+273T>A	ENSP00000499492.1:n.674+273T>A
ENST00000671022.1:n.933T>A
ENST00000244020.4:c.843T>A	ENSP00000244020.3:p.Pro281=
ENST00000483871.6:c.*703T>A	ENSP00000433544.1:n.*703T>A
NM_006275.5:c.843T>A	NP_006266.2:p.Pro281=
NR_034009.1:n.1281T>A
XR_936608.1:n.1602T>A
XR_936608.2:n.1602T>A
NM_006275.6:c.843T>A MANE Select	NP_006266.2:p.Pro281=
NR_034009.2:n.1249T>A