Canonical Allele Identifier: CA409071131

Gene: SRSF6

Linked Data

• MyVariant Identifiers: chr20:g.42089210T>A (hg19) ; chr20:g.43460570T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460570T>A , CM000682.2:g.43460570T>A	GRCh38
NC_000020.10:g.42089210T>A , CM000682.1:g.42089210T>A	GRCh37
NC_000020.9:g.41522624T>A	NCBI36
NG_029906.1:g.7707T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.646T>A MANE Select	ENSP00000244020.3:p.Ser216Thr
ENST00000657241.1:c.626T>A
ENST00000662078.1:c.646T>A	ENSP00000499666.1:p.Ser216Thr
ENST00000668808.1:c.646T>A	ENSP00000499517.1:p.Ser216Thr
ENST00000670741.1:c.646T>A	ENSP00000499492.1:p.Ser216Thr
ENST00000671022.1:n.736T>A
ENST00000244020.4:c.646T>A	ENSP00000244020.3:p.Ser216Thr
ENST00000483871.6:c.*506T>A	ENSP00000433544.1:n.*506T>A
NM_006275.5:c.646T>A	NP_006266.2:p.Ser216Thr
NR_034009.1:n.1084T>A
XR_936608.1:n.1405T>A
XR_936608.2:n.1405T>A
NM_006275.6:c.646T>A MANE Select	NP_006266.2:p.Ser216Thr
NR_034009.2:n.1052T>A