Canonical Allele Identifier: CA409071862

Gene: SRSF6

Linked Data

• MyVariant Identifiers: chr20:g.42089512A>C (hg19) ; chr20:g.43460872A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460872A>C , CM000682.2:g.43460872A>C	GRCh38
NC_000020.10:g.42089512A>C , CM000682.1:g.42089512A>C	GRCh37
NC_000020.9:g.41522926A>C	NCBI36
NG_029906.1:g.8009A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000244020.5:c.844A>C MANE Select	ENSP00000244020.3:p.Lys282Gln
ENST00000657241.1:c.654+274A>C
ENST00000662078.1:c.674+274A>C	ENSP00000499666.1:n.674+274A>C
ENST00000668808.1:c.824+20A>C	ENSP00000499517.1:n.824+20A>C
ENST00000670741.1:c.674+274A>C	ENSP00000499492.1:n.674+274A>C
ENST00000671022.1:n.934A>C
ENST00000244020.4:c.844A>C	ENSP00000244020.3:p.Lys282Gln
ENST00000483871.6:c.*704A>C	ENSP00000433544.1:n.*704A>C
NM_006275.5:c.844A>C	NP_006266.2:p.Lys282Gln
NR_034009.1:n.1282A>C
XR_936608.1:n.1603A>C
XR_936608.2:n.1603A>C
NM_006275.6:c.844A>C MANE Select	NP_006266.2:p.Lys282Gln
NR_034009.2:n.1250A>C