Canonical Allele Identifier: CA363277421
Gene: DCDC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24205021A>G , CM000668.2:g.24205021A>G GRCh38
NC_000006.11:g.24205249A>G , CM000668.1:g.24205249A>G GRCh37
NC_000006.10:g.24313228A>G NCBI36
NG_012829.1:g.158032T>C
NG_012829.2:g.183272T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1004T>C MANE Select ENSP00000367715.3:p.Val335Ala
ENST00000378450.6:c.263T>C ENSP00000367711.3:p.Val88Ala
ENST00000378454.7:c.1004T>C ENSP00000367715.3:p.Val335Ala
NM_001195610.1:c.1004T>C NP_001182539.1:p.Val335Ala
NM_016356.4:c.1004T>C NP_057440.2:p.Val335Ala
NM_016356.5:c.1004T>C MANE Select NP_057440.2:p.Val335Ala
NM_001195610.2:c.1004T>C NP_001182539.1:p.Val335Ala