Canonical Allele Identifier: CA510736996

Gene: SRSF6

Linked Data

• MyVariant Identifiers: chr20:g.42089382A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460742A>G , CM000682.2:g.43460742A>G	GRCh38
NC_000020.10:g.42089382A>G , CM000682.1:g.42089382A>G	GRCh37
NC_000020.9:g.41522796A>G	NCBI36
NG_029906.1:g.7879A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.714A>G MANE Select	ENSP00000244020.3:p.Ser238=
ENST00000657241.1:c.654+144A>G
ENST00000662078.1:c.674+144A>G	ENSP00000499666.1:n.674+144A>G
ENST00000668808.1:c.714A>G	ENSP00000499517.1:p.Ser238=
ENST00000670741.1:c.674+144A>G	ENSP00000499492.1:n.674+144A>G
ENST00000671022.1:n.804A>G
ENST00000244020.4:c.714A>G	ENSP00000244020.3:p.Ser238=
ENST00000483871.6:c.*574A>G	ENSP00000433544.1:n.*574A>G
NM_006275.5:c.714A>G	NP_006266.2:p.Ser238=
NR_034009.1:n.1152A>G
XR_936608.1:n.1473A>G
XR_936608.2:n.1473A>G
NM_006275.6:c.714A>G MANE Select	NP_006266.2:p.Ser238=
NR_034009.2:n.1120A>G