Canonical Allele Identifier: CA363277442

Gene: DCDC2

Linked Data

• COSMIC: COSM4390202 ; COSM4390203
• MyVariant Identifiers: chr6:g.24205258T>A (hg19) ; chr6:g.24205030T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24205030T>A , CM000668.2:g.24205030T>A	GRCh38
NC_000006.11:g.24205258T>A , CM000668.1:g.24205258T>A	GRCh37
NC_000006.10:g.24313237T>A	NCBI36
NG_012829.1:g.158023A>T
NG_012829.2:g.183263A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.995A>T MANE Select	ENSP00000367715.3:p.Asp332Val
ENST00000378450.6:c.254A>T	ENSP00000367711.3:p.Asp85Val
ENST00000378454.7:c.995A>T	ENSP00000367715.3:p.Asp332Val
NM_001195610.1:c.995A>T	NP_001182539.1:p.Asp332Val
NM_016356.4:c.995A>T	NP_057440.2:p.Asp332Val
NM_016356.5:c.995A>T MANE Select	NP_057440.2:p.Asp332Val
NM_001195610.2:c.995A>T	NP_001182539.1:p.Asp332Val