Canonical Allele Identifier: CA2573142191
Gene: DDC HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50544037_50544038delinsCA , CM000669.2:g.50544037_50544038delinsCA GRCh38
NC_000007.13:g.50611735_50611736delinsCA , CM000669.1:g.50611735_50611736delinsCA GRCh37
NC_000007.12:g.50579229_50579230delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000444124.7:c.48_49delinsTG MANE Select ENSP00000403644.2:p.Met17Val
ENST00000357936.9:c.48_49delinsTG ENSP00000350616.5:p.Met17Val
ENST00000380984.4:c.48_49delinsTG ENSP00000370371.4:p.Met17Val
ENST00000420203.1:c.48_49delinsTG ENSP00000408626.1:p.Met17Val
ENST00000426377.5:c.48_49delinsTG ENSP00000395069.1:p.Met17Val
ENST00000431062.5:c.48_49delinsTG ENSP00000399184.1:p.Met17Val
ENST00000444124.6:c.48_49delinsTG ENSP00000403644.2:p.Met17Val
ENST00000444733.5:c.48_49delinsTG ENSP00000393724.1:p.Met17Val
ENST00000615193.4:c.48_49delinsTG ENSP00000484104.1:p.Met17Val
ENST00000617822.4:c.48_49delinsTG ENSP00000478385.1:p.Met17Val
ENST00000622873.4:c.48_49delinsTG ENSP00000479110.1:p.Met17Val
XM_005271745.3:c.48_49delinsTG XP_005271802.1:p.Met17Val
XM_005271745.4:c.48_49delinsTG XP_005271802.1:p.Met17Val
NM_001082971.2:c.48_49delinsTG MANE Select NP_001076440.2:p.Met17Val
NM_000790.4:c.48_49delinsTG NP_000781.2:p.Met17Val
NM_001242888.2:c.48_49delinsTG NP_001229817.2:p.Met17Val
NM_001242890.2:c.48_49delinsTG NP_001229819.2:p.Met17Val
NM_001242886.2:c.48_49delinsTG NP_001229815.2:p.Met17Val
NM_001242887.2:c.48_49delinsTG NP_001229816.2:p.Met17Val
NM_001242889.2:c.48_49delinsTG NP_001229818.2:p.Met17Val
Search 100 bp 5'
Search 100 bp 3'