Canonical Allele Identifier: CA510736932

Gene: SRSF6

Linked Data

• MyVariant Identifiers: chr20:g.42089349G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460709G>A , CM000682.2:g.43460709G>A	GRCh38
NC_000020.10:g.42089349G>A , CM000682.1:g.42089349G>A	GRCh37
NC_000020.9:g.41522763G>A	NCBI36
NG_029906.1:g.7846G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.681G>A MANE Select	ENSP00000244020.3:p.Arg227=
ENST00000657241.1:c.654+111G>A
ENST00000662078.1:c.674+111G>A	ENSP00000499666.1:n.674+111G>A
ENST00000668808.1:c.681G>A	ENSP00000499517.1:p.Arg227=
ENST00000670741.1:c.674+111G>A	ENSP00000499492.1:n.674+111G>A
ENST00000671022.1:n.771G>A
ENST00000244020.4:c.681G>A	ENSP00000244020.3:p.Arg227=
ENST00000483871.6:c.*541G>A	ENSP00000433544.1:n.*541G>A
NM_006275.5:c.681G>A	NP_006266.2:p.Arg227=
NR_034009.1:n.1119G>A
XR_936608.1:n.1440G>A
XR_936608.2:n.1440G>A
NM_006275.6:c.681G>A MANE Select	NP_006266.2:p.Arg227=
NR_034009.2:n.1087G>A