Canonical Allele Identifier: CA510737332

Gene: SRSF6

Linked Data

• MyVariant Identifiers: chr20:g.42089523A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460883A>T , CM000682.2:g.43460883A>T	GRCh38
NC_000020.10:g.42089523A>T , CM000682.1:g.42089523A>T	GRCh37
NC_000020.9:g.41522937A>T	NCBI36
NG_029906.1:g.8020A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000244020.5:c.855A>T MANE Select	ENSP00000244020.3:p.Gly285=
ENST00000657241.1:c.654+285A>T
ENST00000662078.1:c.674+285A>T	ENSP00000499666.1:n.674+285A>T
ENST00000668808.1:c.824+31A>T	ENSP00000499517.1:n.824+31A>T
ENST00000670741.1:c.674+285A>T	ENSP00000499492.1:n.674+285A>T
ENST00000671022.1:n.945A>T
ENST00000244020.4:c.855A>T	ENSP00000244020.3:p.Gly285=
ENST00000483871.6:c.*715A>T	ENSP00000433544.1:n.*715A>T
NM_006275.5:c.855A>T	NP_006266.2:p.Gly285=
NR_034009.1:n.1293A>T
XR_936608.1:n.1614A>T
XR_936608.2:n.1614A>T
NM_006275.6:c.855A>T MANE Select	NP_006266.2:p.Gly285=
NR_034009.2:n.1261A>T