Canonical Allele Identifier: CA2519485049

Gene: ODAD2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27862005_27862006insC , CM000672.2:g.27862005_27862006insC	GRCh38
NC_000010.10:g.28150934_28150935insC , CM000672.1:g.28150934_28150935insC	GRCh37
NC_000010.9:g.28190940_28190941insC	NCBI36
NG_042820.1:g.142045_142046insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.2799+428_2799+429insG MANE Select	ENSP00000306410.5:n.2799+428_2799+429insG
ENST00000672841.1:c.1875+428_1875+429insG	ENSP00000499983.1:n.1875+428_1875+429insG
ENST00000672877.1:c.1374+428_1374+429insG	ENSP00000500120.1:n.1374+428_1374+429insG
ENST00000673384.1:c.1875+428_1875+429insG	ENSP00000500856.1:n.1875+428_1875+429insG
ENST00000673439.1:c.2799+428_2799+429insG	ENSP00000500782.1:n.2799+428_2799+429insG
ENST00000305242.9:c.2799+428_2799+429insG	ENSP00000306410.5:n.2799+428_2799+429insG
NM_001290020.1:c.2799+428_2799+429insG	NP_001276949.1:n.2799+428_2799+429insG
NM_001290021.1:c.1374+428_1374+429insG	NP_001276950.1:n.1374+428_1374+429insG
NM_001312689.1:c.1875+428_1875+429insG	NP_001299618.1:n.1875+428_1875+429insG
NM_018076.3:c.2799+428_2799+429insG	NP_060546.2:n.2799+428_2799+429insG
NM_018076.4:c.2799+428_2799+429insG	NP_060546.2:n.2799+428_2799+429insG
XM_011519526.1:c.2799+428_2799+429insG	XP_011517828.1:n.2799+428_2799+429insG
XM_011519527.1:c.2799+428_2799+429insG	XP_011517829.1:n.2799+428_2799+429insG
XM_011519528.1:c.2799+428_2799+429insG	XP_011517830.1:n.2799+428_2799+429insG
XM_011519529.1:c.2799+428_2799+429insG	XP_011517831.1:n.2799+428_2799+429insG
XM_011519530.1:c.2799+428_2799+429insG	XP_011517832.1:n.2799+428_2799+429insG
XM_011519531.1:c.2799+428_2799+429insG	XP_011517833.1:n.2799+428_2799+429insG
XM_011519532.1:c.2589+428_2589+429insG	XP_011517834.1:n.2589+428_2589+429insG
XM_011519533.1:c.1875+428_1875+429insG	XP_011517835.1:n.1875+428_1875+429insG
XM_011519534.1:c.1875+428_1875+429insG	XP_011517836.1:n.1875+428_1875+429insG
XM_011519535.1:c.1713+428_1713+429insG	XP_011517837.1:n.1713+428_1713+429insG
XM_011519537.1:c.1374+428_1374+429insG	XP_011517839.1:n.1374+428_1374+429insG
XM_024448049.1:c.2928+428_2928+429insG	XP_024303817.1:n.2928+428_2928+429insG
XM_024448050.1:c.2928+428_2928+429insG	XP_024303818.1:n.2928+428_2928+429insG
XM_024448051.1:c.2928+428_2928+429insG	XP_024303819.1:n.2928+428_2928+429insG
XM_024448052.1:c.2928+428_2928+429insG	XP_024303820.1:n.2928+428_2928+429insG
XM_024448053.1:c.2928+428_2928+429insG	XP_024303821.1:n.2928+428_2928+429insG
XM_024448054.1:c.2718+428_2718+429insG	XP_024303822.1:n.2718+428_2718+429insG
XM_024448055.1:c.2004+428_2004+429insG	XP_024303823.1:n.2004+428_2004+429insG
XM_024448056.1:c.2004+428_2004+429insG	XP_024303824.1:n.2004+428_2004+429insG
XM_024448057.1:c.1842+428_1842+429insG	XP_024303825.1:n.1842+428_1842+429insG
XM_024448058.1:c.1503+428_1503+429insG	XP_024303826.1:n.1503+428_1503+429insG
NM_001290020.2:c.2799+428_2799+429insG	NP_001276949.1:n.2799+428_2799+429insG
NM_001290021.2:c.1374+428_1374+429insG	NP_001276950.1:n.1374+428_1374+429insG
NM_001312689.2:c.1875+428_1875+429insG	NP_001299618.1:n.1875+428_1875+429insG
NM_018076.5:c.2799+428_2799+429insG MANE Select	NP_060546.2:n.2799+428_2799+429insG