Canonical Allele Identifier: CA9432249
Community Standard Title: NM_203486.3(DLL3):c.677C>G (p.Pro226Arg)
Gene: DLL3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39504095C>G , CM000681.2:g.39504095C>G GRCh38
NC_000019.9:g.39994735C>G , CM000681.1:g.39994735C>G GRCh37
NC_000019.8:g.44686575C>G NCBI36
NG_008256.1:g.10179C>G

Transcript Alleles

HGVS Amino-acid Change
NM_203486.3:c.677C>G MANE Select NP_982353.1:p.Pro226Arg
ENST00000356433.10:c.677C>G MANE Select ENSP00000348810.4:p.Pro226Arg
NM_016941.3:c.677C>G NP_058637.1:p.Pro226Arg
NM_016941.4:c.677C>G NP_058637.1:p.Pro226Arg
NM_203486.2:c.677C>G NP_982353.1:p.Pro226Arg
ENST00000205143.4:c.677C>G ENSP00000205143.3:p.Pro226Arg
ENST00000356433.9:c.677C>G ENSP00000348810.4:p.Pro226Arg
ENST00000596614.5:c.410-2944C>G ENSP00000471688.1:n.410-2944C>G
ENST00000600437.1:n.757C>G
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