Canonical Allele Identifier: CA510565256

Gene: SRSF6

Linked Data

• MyVariant Identifiers: chr20:g.42089218T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460578T>C , CM000682.2:g.43460578T>C	GRCh38
NC_000020.10:g.42089218T>C , CM000682.1:g.42089218T>C	GRCh37
NC_000020.9:g.41522632T>C	NCBI36
NG_029906.1:g.7715T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.654T>C MANE Select	ENSP00000244020.3:p.Ser218=
ENST00000657241.1:c.634T>C
ENST00000662078.1:c.654T>C	ENSP00000499666.1:p.Ser218=
ENST00000668808.1:c.654T>C	ENSP00000499517.1:p.Ser218=
ENST00000670741.1:c.654T>C	ENSP00000499492.1:p.Ser218=
ENST00000671022.1:n.744T>C
ENST00000244020.4:c.654T>C	ENSP00000244020.3:p.Ser218=
ENST00000483871.6:c.*514T>C	ENSP00000433544.1:n.*514T>C
NM_006275.5:c.654T>C	NP_006266.2:p.Ser218=
NR_034009.1:n.1092T>C
XR_936608.1:n.1413T>C
XR_936608.2:n.1413T>C
NM_006275.6:c.654T>C MANE Select	NP_006266.2:p.Ser218=
NR_034009.2:n.1060T>C