Canonical Allele Identifier: CA566291272
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1479076774
gnomAD v2: 6-24278257-GATAATA-G
gnomAD v3: 6-24278029-GATAATA-G
gnomAD v4: 6-24278029-GATAATA-G
MyVariant Identifiers: chr6:g.24278258_24278263del (hg19) chr6:g.24278030_24278035del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278034_24278039del , CM000668.2:g.24278034_24278039del GRCh38
NC_000006.11:g.24278262_24278267del , CM000668.1:g.24278262_24278267del GRCh37
NC_000006.10:g.24386241_24386246del NCBI36
NG_012829.1:g.85018_85023del
NG_012829.2:g.110258_110263del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.922+14_922+19del MANE Select ENSP00000367715.3:n.922+14_922+19del
ENST00000378454.7:c.922+14_922+19del ENSP00000367715.3:n.922+14_922+19del
NM_001195610.1:c.922+14_922+19del NP_001182539.1:n.922+14_922+19del
NM_016356.4:c.922+14_922+19del NP_057440.2:n.922+14_922+19del
NM_016356.5:c.922+14_922+19del MANE Select NP_057440.2:n.922+14_922+19del
NM_001195610.2:c.922+14_922+19del NP_001182539.1:n.922+14_922+19del
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