Canonical Allele Identifier: CA136625643

Gene: DCDC2

Linked Data

• dbSNP Id: rs35916782
• MyVariant Identifiers: chr6:g.24204846_24204847insA (hg19) ; chr6:g.24204618_24204619insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24204621dup , CM000668.2:g.24204621dup	GRCh38
NC_000006.11:g.24204849dup , CM000668.1:g.24204849dup	GRCh37
NC_000006.10:g.24312828dup	NCBI36
NG_012829.1:g.158434dup
NG_012829.2:g.183674dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.1023+383dup MANE Select	ENSP00000367715.3:n.1023+383dup
ENST00000378450.6:c.282+383dup	ENSP00000367711.3:n.282+383dup
ENST00000378454.7:c.1023+383dup	ENSP00000367715.3:n.1023+383dup
NM_001195610.1:c.1023+383dup	NP_001182539.1:n.1023+383dup
NM_016356.4:c.1023+383dup	NP_057440.2:n.1023+383dup
NM_016356.5:c.1023+383dup MANE Select	NP_057440.2:n.1023+383dup
NM_001195610.2:c.1023+383dup	NP_001182539.1:n.1023+383dup