Canonical Allele Identifier: CA2577401498

Gene: SRSF6

Linked Data

• gnomAD v4: 20-43460646-ATGGAGTATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.43460649_43460657del , CM000682.2:g.43460649_43460657del	GRCh38
NC_000020.10:g.42089289_42089297del , CM000682.1:g.42089289_42089297del	GRCh37
NC_000020.9:g.41522703_41522711del	NCBI36
NG_029906.1:g.7786_7794del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244020.5:c.674+51_675-46del MANE Select	ENSP00000244020.3:n.674+51_675-46del
ENST00000657241.1:c.654+51_654+59del
ENST00000662078.1:c.674+51_674+59del	ENSP00000499666.1:n.674+51_674+59del
ENST00000668808.1:c.674+51_675-46del	ENSP00000499517.1:n.674+51_675-46del
ENST00000670741.1:c.674+51_674+59del	ENSP00000499492.1:n.674+51_674+59del
ENST00000671022.1:n.764+51_765-46del
ENST00000244020.4:c.674+51_675-46del	ENSP00000244020.3:n.674+51_675-46del
ENST00000483871.6:c.*534+51_*535-46del	ENSP00000433544.1:n.*534+51_*535-46del
NM_006275.5:c.674+51_675-46del	NP_006266.2:n.674+51_675-46del
NR_034009.1:n.1112+51_1113-46del
XR_936608.1:n.1433+51_1434-46del
XR_936608.2:n.1433+51_1434-46del
NM_006275.6:c.674+51_675-46del MANE Select	NP_006266.2:n.674+51_675-46del
NR_034009.2:n.1080+51_1081-46del