Canonical Allele Identifier: CA314557512

Gene: SRSF6

Linked Data

• dbSNP Id: rs936370890
• MyVariant Identifiers: chr20:g.42089424G>A (hg19) ; chr20:g.43460784G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.756G>A MANE Select	ENSP00000244020.3:p.Lys252=
ENST00000657241.1:c.654+186G>A
ENST00000662078.1:c.674+186G>A	ENSP00000499666.1:n.674+186G>A
ENST00000668808.1:c.756G>A	ENSP00000499517.1:p.Lys252=
ENST00000670741.1:c.674+186G>A	ENSP00000499492.1:n.674+186G>A
ENST00000671022.1:n.846G>A
ENST00000244020.4:c.756G>A	ENSP00000244020.3:p.Lys252=
ENST00000483871.6:c.*616G>A	ENSP00000433544.1:n.*616G>A
NM_006275.5:c.756G>A	NP_006266.2:p.Lys252=
NR_034009.1:n.1194G>A
XR_936608.1:n.1515G>A
XR_936608.2:n.1515G>A
NM_006275.6:c.756G>A MANE Select	NP_006266.2:p.Lys252=
NR_034009.2:n.1162G>A