Canonical Allele Identifier: CA405789172
Gene: DLL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507465G>C , CM000681.2:g.39507465G>C GRCh38
NC_000019.9:g.39998105G>C , CM000681.1:g.39998105G>C GRCh37
NC_000019.8:g.44689945G>C NCBI36
NG_008256.1:g.13549G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000356433.10:c.1520G>C MANE Select ENSP00000348810.4:p.Gly507Ala
ENST00000205143.4:c.1520G>C ENSP00000205143.3:p.Gly507Ala
ENST00000356433.9:c.1520G>C ENSP00000348810.4:p.Gly507Ala
NM_016941.3:c.1520G>C NP_058637.1:p.Gly507Ala
NM_203486.2:c.1520G>C NP_982353.1:p.Gly507Ala
NM_016941.4:c.1520G>C NP_058637.1:p.Gly507Ala
NM_203486.3:c.1520G>C MANE Select NP_982353.1:p.Gly507Ala