Canonical Allele Identifier: CA409071468

Gene: SRSF6

Linked Data

• gnomAD v4: 20-43460766-G-C
• MyVariant Identifiers: chr20:g.42089406G>C (hg19) ; chr20:g.43460766G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460766G>C , CM000682.2:g.43460766G>C	GRCh38
NC_000020.10:g.42089406G>C , CM000682.1:g.42089406G>C	GRCh37
NC_000020.9:g.41522820G>C	NCBI36
NG_029906.1:g.7903G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.738G>C MANE Select	ENSP00000244020.3:p.Lys246Asn
ENST00000657241.1:c.654+168G>C
ENST00000662078.1:c.674+168G>C	ENSP00000499666.1:n.674+168G>C
ENST00000668808.1:c.738G>C	ENSP00000499517.1:p.Lys246Asn
ENST00000670741.1:c.674+168G>C	ENSP00000499492.1:n.674+168G>C
ENST00000671022.1:n.828G>C
ENST00000244020.4:c.738G>C	ENSP00000244020.3:p.Lys246Asn
ENST00000483871.6:c.*598G>C	ENSP00000433544.1:n.*598G>C
NM_006275.5:c.738G>C	NP_006266.2:p.Lys246Asn
NR_034009.1:n.1176G>C
XR_936608.1:n.1497G>C
XR_936608.2:n.1497G>C
NM_006275.6:c.738G>C MANE Select	NP_006266.2:p.Lys246Asn
NR_034009.2:n.1144G>C