Canonical Allele Identifier: CA2787071696

Gene: ODAD2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27862658_27862659del , CM000672.2:g.27862658_27862659del	GRCh38
NC_000010.10:g.28151587_28151588del , CM000672.1:g.28151587_28151588del	GRCh37
NC_000010.9:g.28191593_28191594del	NCBI36
NG_042820.1:g.141392_141393del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.2611-37_2611-36del MANE Select	ENSP00000306410.5:n.2611-37_2611-36del
ENST00000672841.1:c.1687-37_1687-36del	ENSP00000499983.1:n.1687-37_1687-36del
ENST00000672877.1:c.1186-37_1186-36del	ENSP00000500120.1:n.1186-37_1186-36del
ENST00000673384.1:c.1687-37_1687-36del	ENSP00000500856.1:n.1687-37_1687-36del
ENST00000673439.1:c.2611-37_2611-36del	ENSP00000500782.1:n.2611-37_2611-36del
ENST00000305242.9:c.2611-37_2611-36del	ENSP00000306410.5:n.2611-37_2611-36del
NM_001290020.1:c.2611-37_2611-36del	NP_001276949.1:n.2611-37_2611-36del
NM_001290021.1:c.1186-37_1186-36del	NP_001276950.1:n.1186-37_1186-36del
NM_001312689.1:c.1687-37_1687-36del	NP_001299618.1:n.1687-37_1687-36del
NM_018076.3:c.2611-37_2611-36del	NP_060546.2:n.2611-37_2611-36del
NM_018076.4:c.2611-37_2611-36del	NP_060546.2:n.2611-37_2611-36del
XM_011519526.1:c.2611-37_2611-36del	XP_011517828.1:n.2611-37_2611-36del
XM_011519527.1:c.2611-37_2611-36del	XP_011517829.1:n.2611-37_2611-36del
XM_011519528.1:c.2611-37_2611-36del	XP_011517830.1:n.2611-37_2611-36del
XM_011519529.1:c.2611-37_2611-36del	XP_011517831.1:n.2611-37_2611-36del
XM_011519530.1:c.2611-37_2611-36del	XP_011517832.1:n.2611-37_2611-36del
XM_011519531.1:c.2611-37_2611-36del	XP_011517833.1:n.2611-37_2611-36del
XM_011519532.1:c.2401-37_2401-36del	XP_011517834.1:n.2401-37_2401-36del
XM_011519533.1:c.1687-37_1687-36del	XP_011517835.1:n.1687-37_1687-36del
XM_011519534.1:c.1687-37_1687-36del	XP_011517836.1:n.1687-37_1687-36del
XM_011519535.1:c.1525-37_1525-36del	XP_011517837.1:n.1525-37_1525-36del
XM_011519537.1:c.1186-37_1186-36del	XP_011517839.1:n.1186-37_1186-36del
XM_024448049.1:c.2740-37_2740-36del	XP_024303817.1:n.2740-37_2740-36del
XM_024448050.1:c.2740-37_2740-36del	XP_024303818.1:n.2740-37_2740-36del
XM_024448051.1:c.2740-37_2740-36del	XP_024303819.1:n.2740-37_2740-36del
XM_024448052.1:c.2740-37_2740-36del	XP_024303820.1:n.2740-37_2740-36del
XM_024448053.1:c.2740-37_2740-36del	XP_024303821.1:n.2740-37_2740-36del
XM_024448054.1:c.2530-37_2530-36del	XP_024303822.1:n.2530-37_2530-36del
XM_024448055.1:c.1816-37_1816-36del	XP_024303823.1:n.1816-37_1816-36del
XM_024448056.1:c.1816-37_1816-36del	XP_024303824.1:n.1816-37_1816-36del
XM_024448057.1:c.1654-37_1654-36del	XP_024303825.1:n.1654-37_1654-36del
XM_024448058.1:c.1315-37_1315-36del	XP_024303826.1:n.1315-37_1315-36del
NM_001290020.2:c.2611-37_2611-36del	NP_001276949.1:n.2611-37_2611-36del
NM_001290021.2:c.1186-37_1186-36del	NP_001276950.1:n.1186-37_1186-36del
NM_001312689.2:c.1687-37_1687-36del	NP_001299618.1:n.1687-37_1687-36del
NM_018076.5:c.2611-37_2611-36del MANE Select	NP_060546.2:n.2611-37_2611-36del