Canonical Allele Identifier: CA2593681191
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs2113841562

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24306234dup , CM000668.2:g.24306234dup GRCh38
NC_000006.11:g.24306462dup , CM000668.1:g.24306462dup GRCh37
NC_000006.10:g.24414441dup NCBI36
NG_012829.1:g.56819dup
NG_012829.2:g.82059dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.349-4190dup MANE Select ENSP00000367715.3:n.349-4190dup
ENST00000378454.7:c.349-4190dup ENSP00000367715.3:n.349-4190dup
NM_001195610.1:c.349-4190dup NP_001182539.1:n.349-4190dup
NM_016356.4:c.349-4190dup NP_057440.2:n.349-4190dup
NM_016356.5:c.349-4190dup MANE Select NP_057440.2:n.349-4190dup
NM_001195610.2:c.349-4190dup NP_001182539.1:n.349-4190dup