Canonical Allele Identifier: CA136637347

Gene: DCDC2

Linked Data

• dbSNP Id: rs34658513
• MyVariant Identifiers: chr6:g.24302368_24302369insG (hg19) ; chr6:g.24302140_24302141insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24302141dup , CM000668.2:g.24302141dup	GRCh38
NC_000006.11:g.24302369dup , CM000668.1:g.24302369dup	GRCh37
NC_000006.10:g.24410348dup	NCBI36
NG_012829.1:g.60912dup
NG_012829.2:g.86152dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.349-97dup MANE Select	ENSP00000367715.3:n.349-97dup
ENST00000378454.7:c.349-97dup	ENSP00000367715.3:n.349-97dup
NM_001195610.1:c.349-97dup	NP_001182539.1:n.349-97dup
NM_016356.4:c.349-97dup	NP_057440.2:n.349-97dup
NM_016356.5:c.349-97dup MANE Select	NP_057440.2:n.349-97dup
NM_001195610.2:c.349-97dup	NP_001182539.1:n.349-97dup