Canonical Allele Identifier: CA136625861
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs531683433
gnomAD v2: 6-24206961-CAAATA-C
gnomAD v3: 6-24206733-CAAATA-C
gnomAD v4: 6-24206733-CAAATA-C
MyVariant Identifiers: chr6:g.24206962_24206966del (hg19) chr6:g.24206734_24206738del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206743_24206747del , CM000668.2:g.24206743_24206747del GRCh38
NC_000006.11:g.24206971_24206975del , CM000668.1:g.24206971_24206975del GRCh37
NC_000006.10:g.24314950_24314954del NCBI36
NG_012829.1:g.156315_156319del
NG_012829.2:g.181555_181559del

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-1636_923-1632del MANE Select ENSP00000367715.3:n.923-1636_923-1632del
ENST00000378454.7:c.923-1636_923-1632del ENSP00000367715.3:n.923-1636_923-1632del
NM_001195610.1:c.923-1636_923-1632del NP_001182539.1:n.923-1636_923-1632del
NM_016356.4:c.923-1636_923-1632del NP_057440.2:n.923-1636_923-1632del
NM_016356.5:c.923-1636_923-1632del MANE Select NP_057440.2:n.923-1636_923-1632del
NM_001195610.2:c.923-1636_923-1632del NP_001182539.1:n.923-1636_923-1632del
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