Canonical Allele Identifier: CA2335548872
Gene: DLL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507464G= , CM000681.2:g.39507464G= GRCh38
NC_000019.9:g.39998104G= , CM000681.1:g.39998104G= GRCh37
NC_000019.8:g.44689944G= NCBI36
NG_008256.1:g.13548G=

Transcript Alleles

HGVS Amino-acid change
ENST00000356433.10:c.1519G= MANE Select ENSP00000348810.4:p.Gly507=
ENST00000205143.4:c.1519G= ENSP00000205143.3:p.Gly507=
ENST00000356433.9:c.1519G= ENSP00000348810.4:p.Gly507=
NM_016941.3:c.1519G= NP_058637.1:p.Gly507=
NM_203486.2:c.1519G= NP_982353.1:p.Gly507=
NM_016941.4:c.1519G= NP_058637.1:p.Gly507=
NM_203486.3:c.1519G= MANE Select NP_982353.1:p.Gly507=