Canonical Allele Identifier: CA663429793

Gene: ODAD2

Linked Data

• dbSNP Id: rs1327044617
• gnomAD v3: 10-27862152-TAC-T
• gnomAD v4: 10-27862152-TAC-T
• MyVariant Identifiers: chr10:g.28151082_28151083del (hg19) ; chr10:g.27862153_27862154del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27862154_27862155del , CM000672.2:g.27862154_27862155del	GRCh38
NC_000010.10:g.28151083_28151084del , CM000672.1:g.28151083_28151084del	GRCh37
NC_000010.9:g.28191089_28191090del	NCBI36
NG_042820.1:g.141897_141898del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.2799+280_2799+281del MANE Select	ENSP00000306410.5:n.2799+280_2799+281del
ENST00000672841.1:c.1875+280_1875+281del	ENSP00000499983.1:n.1875+280_1875+281del
ENST00000672877.1:c.1374+280_1374+281del	ENSP00000500120.1:n.1374+280_1374+281del
ENST00000673384.1:c.1875+280_1875+281del	ENSP00000500856.1:n.1875+280_1875+281del
ENST00000673439.1:c.2799+280_2799+281del	ENSP00000500782.1:n.2799+280_2799+281del
ENST00000305242.9:c.2799+280_2799+281del	ENSP00000306410.5:n.2799+280_2799+281del
NM_001290020.1:c.2799+280_2799+281del	NP_001276949.1:n.2799+280_2799+281del
NM_001290021.1:c.1374+280_1374+281del	NP_001276950.1:n.1374+280_1374+281del
NM_001312689.1:c.1875+280_1875+281del	NP_001299618.1:n.1875+280_1875+281del
NM_018076.3:c.2799+280_2799+281del	NP_060546.2:n.2799+280_2799+281del
NM_018076.4:c.2799+280_2799+281del	NP_060546.2:n.2799+280_2799+281del
XM_011519526.1:c.2799+280_2799+281del	XP_011517828.1:n.2799+280_2799+281del
XM_011519527.1:c.2799+280_2799+281del	XP_011517829.1:n.2799+280_2799+281del
XM_011519528.1:c.2799+280_2799+281del	XP_011517830.1:n.2799+280_2799+281del
XM_011519529.1:c.2799+280_2799+281del	XP_011517831.1:n.2799+280_2799+281del
XM_011519530.1:c.2799+280_2799+281del	XP_011517832.1:n.2799+280_2799+281del
XM_011519531.1:c.2799+280_2799+281del	XP_011517833.1:n.2799+280_2799+281del
XM_011519532.1:c.2589+280_2589+281del	XP_011517834.1:n.2589+280_2589+281del
XM_011519533.1:c.1875+280_1875+281del	XP_011517835.1:n.1875+280_1875+281del
XM_011519534.1:c.1875+280_1875+281del	XP_011517836.1:n.1875+280_1875+281del
XM_011519535.1:c.1713+280_1713+281del	XP_011517837.1:n.1713+280_1713+281del
XM_011519537.1:c.1374+280_1374+281del	XP_011517839.1:n.1374+280_1374+281del
XM_024448049.1:c.2928+280_2928+281del	XP_024303817.1:n.2928+280_2928+281del
XM_024448050.1:c.2928+280_2928+281del	XP_024303818.1:n.2928+280_2928+281del
XM_024448051.1:c.2928+280_2928+281del	XP_024303819.1:n.2928+280_2928+281del
XM_024448052.1:c.2928+280_2928+281del	XP_024303820.1:n.2928+280_2928+281del
XM_024448053.1:c.2928+280_2928+281del	XP_024303821.1:n.2928+280_2928+281del
XM_024448054.1:c.2718+280_2718+281del	XP_024303822.1:n.2718+280_2718+281del
XM_024448055.1:c.2004+280_2004+281del	XP_024303823.1:n.2004+280_2004+281del
XM_024448056.1:c.2004+280_2004+281del	XP_024303824.1:n.2004+280_2004+281del
XM_024448057.1:c.1842+280_1842+281del	XP_024303825.1:n.1842+280_1842+281del
XM_024448058.1:c.1503+280_1503+281del	XP_024303826.1:n.1503+280_1503+281del
NM_001290020.2:c.2799+280_2799+281del	NP_001276949.1:n.2799+280_2799+281del
NM_001290021.2:c.1374+280_1374+281del	NP_001276950.1:n.1374+280_1374+281del
NM_001312689.2:c.1875+280_1875+281del	NP_001299618.1:n.1875+280_1875+281del
NM_018076.5:c.2799+280_2799+281del MANE Select	NP_060546.2:n.2799+280_2799+281del