Canonical Allele Identifier: CA592783489

Gene: ODAD2

Linked Data

• dbSNP Id: rs1227849748
• gnomAD v2: 10-28151473-CTTCT-C
• gnomAD v4: 10-27862544-CTTCT-C
• MyVariant Identifiers: chr10:g.28151474_28151477del (hg19) ; chr10:g.27862545_27862548del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27862547_27862550del , CM000672.2:g.27862547_27862550del	GRCh38
NC_000010.10:g.28151476_28151479del , CM000672.1:g.28151476_28151479del	GRCh37
NC_000010.9:g.28191482_28191485del	NCBI36
NG_042820.1:g.141503_141506del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.2685_2688del MANE Select	ENSP00000306410.5:p.Glu896PhefsTer12
ENST00000672841.1:c.1761_1764del	ENSP00000499983.1:p.Glu588PhefsTer12
ENST00000672877.1:c.1260_1263del	ENSP00000500120.1:p.Glu421PhefsTer12
ENST00000673384.1:c.1761_1764del	ENSP00000500856.1:p.Glu588PhefsTer12
ENST00000673439.1:c.2685_2688del	ENSP00000500782.1:p.Glu896PhefsTer12
ENST00000305242.9:c.2685_2688del	ENSP00000306410.5:p.Glu896PhefsTer12
NM_001290020.1:c.2685_2688del	NP_001276949.1:p.Glu896PhefsTer12
NM_001290021.1:c.1260_1263del	NP_001276950.1:p.Glu421PhefsTer12
NM_001312689.1:c.1761_1764del	NP_001299618.1:p.Glu588PhefsTer12
NM_018076.3:c.2685_2688del	NP_060546.2:p.Glu896PhefsTer12
NM_018076.4:c.2685_2688del	NP_060546.2:p.Glu896PhefsTer12
XM_011519526.1:c.2685_2688del	XP_011517828.1:p.Glu896PhefsTer12
XM_011519527.1:c.2685_2688del	XP_011517829.1:p.Glu896PhefsTer12
XM_011519528.1:c.2685_2688del	XP_011517830.1:p.Glu896PhefsTer12
XM_011519529.1:c.2685_2688del	XP_011517831.1:p.Glu896PhefsTer12
XM_011519530.1:c.2685_2688del	XP_011517832.1:p.Glu896PhefsTer12
XM_011519531.1:c.2685_2688del	XP_011517833.1:p.Glu896PhefsTer12
XM_011519532.1:c.2475_2478del	XP_011517834.1:p.Glu826PhefsTer12
XM_011519533.1:c.1761_1764del	XP_011517835.1:p.Glu588PhefsTer12
XM_011519534.1:c.1761_1764del	XP_011517836.1:p.Glu588PhefsTer12
XM_011519535.1:c.1599_1602del	XP_011517837.1:p.Glu534PhefsTer12
XM_011519537.1:c.1260_1263del	XP_011517839.1:p.Glu421PhefsTer12
XM_024448049.1:c.2814_2817del	XP_024303817.1:p.Glu939PhefsTer12
XM_024448050.1:c.2814_2817del	XP_024303818.1:p.Glu939PhefsTer12
XM_024448051.1:c.2814_2817del	XP_024303819.1:p.Glu939PhefsTer12
XM_024448052.1:c.2814_2817del	XP_024303820.1:p.Glu939PhefsTer12
XM_024448053.1:c.2814_2817del	XP_024303821.1:p.Glu939PhefsTer12
XM_024448054.1:c.2604_2607del	XP_024303822.1:p.Glu869PhefsTer12
XM_024448055.1:c.1890_1893del	XP_024303823.1:p.Glu631PhefsTer12
XM_024448056.1:c.1890_1893del	XP_024303824.1:p.Glu631PhefsTer12
XM_024448057.1:c.1728_1731del	XP_024303825.1:p.Glu577PhefsTer12
XM_024448058.1:c.1389_1392del	XP_024303826.1:p.Glu464PhefsTer12
NM_001290020.2:c.2685_2688del	NP_001276949.1:p.Glu896PhefsTer12
NM_001290021.2:c.1260_1263del	NP_001276950.1:p.Glu421PhefsTer12
NM_001312689.2:c.1761_1764del	NP_001299618.1:p.Glu588PhefsTer12
NM_018076.5:c.2685_2688del MANE Select	NP_060546.2:p.Glu896PhefsTer12