Canonical Allele Identifier: CA409071232

Gene: SRSF6

Linked Data

• MyVariant Identifiers: chr20:g.42089342G>T (hg19) ; chr20:g.43460702G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460702G>T , CM000682.2:g.43460702G>T	GRCh38
NC_000020.10:g.42089342G>T , CM000682.1:g.42089342G>T	GRCh37
NC_000020.9:g.41522756G>T	NCBI36
NG_029906.1:g.7839G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.675-1G>T MANE Select	ENSP00000244020.3:n.675-1G>T
ENST00000657241.1:c.654+104G>T
ENST00000662078.1:c.674+104G>T	ENSP00000499666.1:n.674+104G>T
ENST00000668808.1:c.675-1G>T	ENSP00000499517.1:n.675-1G>T
ENST00000670741.1:c.674+104G>T	ENSP00000499492.1:n.674+104G>T
ENST00000671022.1:n.765-1G>T
ENST00000244020.4:c.675-1G>T	ENSP00000244020.3:n.675-1G>T
ENST00000483871.6:c.*535-1G>T	ENSP00000433544.1:n.*535-1G>T
NM_006275.5:c.675-1G>T	NP_006266.2:n.675-1G>T
NR_034009.1:n.1113-1G>T
XR_936608.1:n.1434-1G>T
XR_936608.2:n.1434-1G>T
NM_006275.6:c.675-1G>T MANE Select	NP_006266.2:n.675-1G>T
NR_034009.2:n.1081-1G>T