Canonical Allele Identifier: CA783271438

Gene: ODAD3

Linked Data

• dbSNP Id: rs1484379395
• gnomAD v3: 19-11422678-TCCCCAGAG-T
• gnomAD v4: 19-11422678-TCCCCAGAG-T
• MyVariant Identifiers: chr19:g.11533347_11533354del (hg19) ; chr19:g.11422679_11422686del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422683_11422690del , CM000681.2:g.11422683_11422690del	GRCh38
NC_000019.9:g.11533351_11533358del , CM000681.1:g.11533351_11533358del	GRCh37
NC_000019.8:g.11394351_11394358del	NCBI36
NG_041777.1:g.18097_18104del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1277+15_1277+22del MANE Select	ENSP00000348757.3:n.1277+15_1277+22del
ENST00000356392.8:c.1277+15_1277+22del	ENSP00000348757.3:n.1277+15_1277+22del
ENST00000586836.5:c.704+15_704+22del	ENSP00000467429.1:n.704+15_704+22del
ENST00000591179.5:c.1097+15_1097+22del	ENSP00000466800.1:n.1097+15_1097+22del
ENST00000591345.5:c.*1196+15_*1196+22del	ENSP00000467313.1:n.*1196+15_*1196+22del
NM_001302453.1:c.1115+15_1115+22del	NP_001289382.1:n.1115+15_1115+22del
NM_001302454.1:c.1097+15_1097+22del	NP_001289383.1:n.1097+15_1097+22del
NM_145045.4:c.1277+15_1277+22del	NP_659482.3:n.1277+15_1277+22del
NM_145045.5:c.1277+15_1277+22del MANE Select	NP_659482.3:n.1277+15_1277+22del
NM_001302454.2:c.1097+15_1097+22del	NP_001289383.1:n.1097+15_1097+22del