Canonical Allele Identifier: CA363279856
Gene: DCDC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178394T>C , CM000668.2:g.24178394T>C GRCh38
NC_000006.11:g.24178622T>C , CM000668.1:g.24178622T>C GRCh37
NC_000006.10:g.24286601T>C NCBI36
NG_012829.1:g.184659A>G
NG_012829.2:g.209899A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1262A>G MANE Select ENSP00000367715.3:p.Asn421Ser
ENST00000378450.6:c.521A>G ENSP00000367711.3:p.Asn174Ser
ENST00000378454.7:c.1262A>G ENSP00000367715.3:p.Asn421Ser
NM_001195610.1:c.1262A>G NP_001182539.1:p.Asn421Ser
NM_016356.4:c.1262A>G NP_057440.2:p.Asn421Ser
NM_016356.5:c.1262A>G MANE Select NP_057440.2:p.Asn421Ser
NM_001195610.2:c.1262A>G NP_001182539.1:p.Asn421Ser