Canonical Allele Identifier: CA566221504

Gene: DCDC2

Linked Data

• dbSNP Id: rs1561881965
• gnomAD v2: 6-24185894-GTTTTACACCCATCCATACACATACACACACACACACACACACACACACACACACACACACATATACACACAGATAAAA-G
• gnomAD v3: 6-24185666-GTTTTACACCCATCCATACACATACACACACACACACACACACACACACACACACACACACATATACACACAGATAAAA-G
• gnomAD v4: 6-24185666-GTTTTACACCCATCCATACACATACACACACACACACACACACACACACACACACACACACATATACACACAGATAAAA-G
• MyVariant Identifiers: chr6:g.24185895_24185972del (hg19) ; chr6:g.24185667_24185744del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24185668_24185745del , CM000668.2:g.24185668_24185745del	GRCh38
NC_000006.11:g.24185896_24185973del , CM000668.1:g.24185896_24185973del	GRCh37
NC_000006.10:g.24293875_24293952del	NCBI36
NG_012829.1:g.177309_177386del
NG_012829.2:g.202549_202626del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.1024-7112_1024-7035del MANE Select	ENSP00000367715.3:n.1024-7112_1024-7035del
ENST00000378450.6:c.283-7112_283-7035del	ENSP00000367711.3:n.283-7112_283-7035del
ENST00000378454.7:c.1024-7112_1024-7035del	ENSP00000367715.3:n.1024-7112_1024-7035del
NM_001195610.1:c.1024-7112_1024-7035del	NP_001182539.1:n.1024-7112_1024-7035del
NM_016356.4:c.1024-7112_1024-7035del	NP_057440.2:n.1024-7112_1024-7035del
NM_016356.5:c.1024-7112_1024-7035del MANE Select	NP_057440.2:n.1024-7112_1024-7035del
NM_001195610.2:c.1024-7112_1024-7035del	NP_001182539.1:n.1024-7112_1024-7035del