Canonical Allele Identifier: CA363281193
Gene: DCDC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301971A>C , CM000668.2:g.24301971A>C GRCh38
NC_000006.11:g.24302199A>C , CM000668.1:g.24302199A>C GRCh37
NC_000006.10:g.24410178A>C NCBI36
NG_012829.1:g.61082T>G
NG_012829.2:g.86322T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.422T>G MANE Select ENSP00000367715.3:p.Ile141Ser
ENST00000378454.7:c.422T>G ENSP00000367715.3:p.Ile141Ser
NM_001195610.1:c.422T>G NP_001182539.1:p.Ile141Ser
NM_016356.4:c.422T>G NP_057440.2:p.Ile141Ser
NM_016356.5:c.422T>G MANE Select NP_057440.2:p.Ile141Ser
NM_001195610.2:c.422T>G NP_001182539.1:p.Ile141Ser