Canonical Allele Identifier: CA2365324066

Gene: SRSF6

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460635_43460638delinsCGTA , CM000682.2:g.43460635_43460638delinsCGTA	GRCh38
NC_000020.10:g.42089275_42089278delinsCGTA , CM000682.1:g.42089275_42089278delinsCGTA	GRCh37
NC_000020.9:g.41522689_41522692delinsCGTA	NCBI36
NG_029906.1:g.7772_7775delinsCGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.674+37_674+40delinsCGTA MANE Select	ENSP00000244020.3:n.674+37_674+40delinsCGTA
ENST00000657241.1:c.654+37_654+40delinsCGTA
ENST00000662078.1:c.674+37_674+40delinsCGTA	ENSP00000499666.1:n.674+37_674+40delinsCGTA
ENST00000668808.1:c.674+37_674+40delinsCGTA	ENSP00000499517.1:n.674+37_674+40delinsCGTA
ENST00000670741.1:c.674+37_674+40delinsCGTA	ENSP00000499492.1:n.674+37_674+40delinsCGTA
ENST00000671022.1:n.764+37_764+40delinsCGTA
ENST00000244020.4:c.674+37_674+40delinsCGTA	ENSP00000244020.3:n.674+37_674+40delinsCGTA
ENST00000483871.6:c.*534+37_*534+40delinsCGTA	ENSP00000433544.1:n.*534+37_*534+40delinsCGTA
NM_006275.5:c.674+37_674+40delinsCGTA	NP_006266.2:n.674+37_674+40delinsCGTA
NR_034009.1:n.1112+37_1112+40delinsCGTA
XR_936608.1:n.1433+37_1433+40delinsCGTA
XR_936608.2:n.1433+37_1433+40delinsCGTA
NM_006275.6:c.674+37_674+40delinsCGTA MANE Select	NP_006266.2:n.674+37_674+40delinsCGTA
NR_034009.2:n.1080+37_1080+40delinsCGTA