Canonical Allele Identifier: CA823298121
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1205262915
gnomAD v3: 6-24302145-TC-T
gnomAD v4: 6-24302145-TC-T
MyVariant Identifiers: chr6:g.24302374del (hg19) chr6:g.24302146del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24302147del , CM000668.2:g.24302147del GRCh38
NC_000006.11:g.24302375del , CM000668.1:g.24302375del GRCh37
NC_000006.10:g.24410354del NCBI36
NG_012829.1:g.60907del
NG_012829.2:g.86147del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.349-102del MANE Select ENSP00000367715.3:n.349-102del
ENST00000378454.7:c.349-102del ENSP00000367715.3:n.349-102del
NM_001195610.1:c.349-102del NP_001182539.1:n.349-102del
NM_016356.4:c.349-102del NP_057440.2:n.349-102del
NM_016356.5:c.349-102del MANE Select NP_057440.2:n.349-102del
NM_001195610.2:c.349-102del NP_001182539.1:n.349-102del
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