Canonical Allele Identifier: CA363278539

Gene: DCDC2

Linked Data

• gnomAD v4: 6-24174744-C-A
• MyVariant Identifiers: chr6:g.24174972C>A (hg19) ; chr6:g.24174744C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24174744C>A , CM000668.2:g.24174744C>A	GRCh38
NC_000006.11:g.24174972C>A , CM000668.1:g.24174972C>A	GRCh37
NC_000006.10:g.24282951C>A	NCBI36
NG_012829.1:g.188309G>T
NG_012829.2:g.213549G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.1417G>T MANE Select	ENSP00000367715.3:p.Ala473Ser
ENST00000378450.6:c.676G>T	ENSP00000367711.3:p.Ala226Ser
ENST00000378454.7:c.1417G>T	ENSP00000367715.3:p.Ala473Ser
NM_001195610.1:c.1417G>T	NP_001182539.1:p.Ala473Ser
NM_016356.4:c.1417G>T	NP_057440.2:p.Ala473Ser
NM_016356.5:c.1417G>T MANE Select	NP_057440.2:p.Ala473Ser
NM_001195610.2:c.1417G>T	NP_001182539.1:p.Ala473Ser