Canonical Allele Identifier: CA744599751

Gene: SRSF6

Linked Data

• dbSNP Id: rs1158242754
• MyVariant Identifiers: chr20:g.42089276_42089278del (hg19) ; chr20:g.43460636_43460638del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460636_43460638del , CM000682.2:g.43460636_43460638del	GRCh38
NC_000020.10:g.42089276_42089278del , CM000682.1:g.42089276_42089278del	GRCh37
NC_000020.9:g.41522690_41522692del	NCBI36
NG_029906.1:g.7773_7775del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.674+38_674+40del MANE Select	ENSP00000244020.3:n.674+38_674+40del
ENST00000657241.1:c.654+38_654+40del
ENST00000662078.1:c.674+38_674+40del	ENSP00000499666.1:n.674+38_674+40del
ENST00000668808.1:c.674+38_674+40del	ENSP00000499517.1:n.674+38_674+40del
ENST00000670741.1:c.674+38_674+40del	ENSP00000499492.1:n.674+38_674+40del
ENST00000671022.1:n.764+38_764+40del
ENST00000244020.4:c.674+38_674+40del	ENSP00000244020.3:n.674+38_674+40del
ENST00000483871.6:c.*534+38_*534+40del	ENSP00000433544.1:n.*534+38_*534+40del
NM_006275.5:c.674+38_674+40del	NP_006266.2:n.674+38_674+40del
NR_034009.1:n.1112+38_1112+40del
XR_936608.1:n.1433+38_1433+40del
XR_936608.2:n.1433+38_1433+40del
NM_006275.6:c.674+38_674+40del MANE Select	NP_006266.2:n.674+38_674+40del
NR_034009.2:n.1080+38_1080+40del