Canonical Allele Identifier: CA510565250

Gene: SRSF6

Linked Data

• MyVariant Identifiers: chr20:g.42089212T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460572T>C , CM000682.2:g.43460572T>C	GRCh38
NC_000020.10:g.42089212T>C , CM000682.1:g.42089212T>C	GRCh37
NC_000020.9:g.41522626T>C	NCBI36
NG_029906.1:g.7709T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.648T>C MANE Select	ENSP00000244020.3:p.Ser216=
ENST00000657241.1:c.628T>C
ENST00000662078.1:c.648T>C	ENSP00000499666.1:p.Ser216=
ENST00000668808.1:c.648T>C	ENSP00000499517.1:p.Ser216=
ENST00000670741.1:c.648T>C	ENSP00000499492.1:p.Ser216=
ENST00000671022.1:n.738T>C
ENST00000244020.4:c.648T>C	ENSP00000244020.3:p.Ser216=
ENST00000483871.6:c.*508T>C	ENSP00000433544.1:n.*508T>C
NM_006275.5:c.648T>C	NP_006266.2:p.Ser216=
NR_034009.1:n.1086T>C
XR_936608.1:n.1407T>C
XR_936608.2:n.1407T>C
NM_006275.6:c.648T>C MANE Select	NP_006266.2:p.Ser216=
NR_034009.2:n.1054T>C