Canonical Allele Identifier: CA363280299

Gene: DCDC2

Linked Data

• gnomAD v4: 6-24178491-C-A
• MyVariant Identifiers: chr6:g.24178719C>A (hg19) ; chr6:g.24178491C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24178491C>A , CM000668.2:g.24178491C>A	GRCh38
NC_000006.11:g.24178719C>A , CM000668.1:g.24178719C>A	GRCh37
NC_000006.10:g.24286698C>A	NCBI36
NG_012829.1:g.184562G>T
NG_012829.2:g.209802G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.1165G>T MANE Select	ENSP00000367715.3:p.Glu389Ter
ENST00000378450.6:c.424G>T	ENSP00000367711.3:p.Glu142Ter
ENST00000378454.7:c.1165G>T	ENSP00000367715.3:p.Glu389Ter
NM_001195610.1:c.1165G>T	NP_001182539.1:p.Glu389Ter
NM_016356.4:c.1165G>T	NP_057440.2:p.Glu389Ter
NM_016356.5:c.1165G>T MANE Select	NP_057440.2:p.Glu389Ter
NM_001195610.2:c.1165G>T	NP_001182539.1:p.Glu389Ter