Canonical Allele Identifier: CA1086921789

Gene: DCDC2

Linked Data

• dbSNP Id: rs1760962618
• gnomAD v3: 6-24177982-TCTTAA-T
• gnomAD v4: 6-24177982-TCTTAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24177987_24177991del , CM000668.2:g.24177987_24177991del	GRCh38
NC_000006.11:g.24178215_24178219del , CM000668.1:g.24178215_24178219del	GRCh37
NC_000006.10:g.24286194_24286198del	NCBI36
NG_012829.1:g.185066_185070del
NG_012829.2:g.210306_210310del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.1326+343_1326+347del MANE Select	ENSP00000367715.3:n.1326+343_1326+347del
ENST00000378450.6:c.585+343_585+347del	ENSP00000367711.3:n.585+343_585+347del
ENST00000378454.7:c.1326+343_1326+347del	ENSP00000367715.3:n.1326+343_1326+347del
NM_001195610.1:c.1326+343_1326+347del	NP_001182539.1:n.1326+343_1326+347del
NM_016356.4:c.1326+343_1326+347del	NP_057440.2:n.1326+343_1326+347del
NM_016356.5:c.1326+343_1326+347del MANE Select	NP_057440.2:n.1326+343_1326+347del
NM_001195610.2:c.1326+343_1326+347del	NP_001182539.1:n.1326+343_1326+347del