Canonical Allele Identifier: CA376398267

Gene: ODAD2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27995037C>T , CM000672.2:g.27995037C>T	GRCh38
NC_000010.10:g.28283966C>T , CM000672.1:g.28283966C>T	GRCh37
NC_000010.9:g.28323972C>T	NCBI36
NG_042820.1:g.9014G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.106G>A MANE Select	ENSP00000306410.5:p.Val36Met
ENST00000486279.2:c.106G>A	ENSP00000473438.2:p.Val36Met
ENST00000673439.1:c.106G>A	ENSP00000500782.1:p.Val36Met
ENST00000305242.9:c.106G>A	ENSP00000306410.5:p.Val36Met
ENST00000486279.1:c.106G>A	ENSP00000473438.1:p.Val36Met
NM_001290020.1:c.106G>A	NP_001276949.1:p.Val36Met
NM_018076.3:c.106G>A	NP_060546.2:p.Val36Met
NM_018076.4:c.106G>A	NP_060546.2:p.Val36Met
XM_011519526.1:c.106G>A	XP_011517828.1:p.Val36Met
XM_011519527.1:c.106G>A	XP_011517829.1:p.Val36Met
XM_011519528.1:c.106G>A	XP_011517830.1:p.Val36Met
XM_011519529.1:c.106G>A	XP_011517831.1:p.Val36Met
XM_011519530.1:c.106G>A	XP_011517832.1:p.Val36Met
XM_011519531.1:c.106G>A	XP_011517833.1:p.Val36Met
XM_011519532.1:c.106G>A	XP_011517834.1:p.Val36Met
XM_011519536.1:c.106G>A	XP_011517838.1:p.Val36Met
XM_017016371.1:c.106G>A	XP_016871860.1:p.Val36Met
XM_024448049.1:c.106G>A	XP_024303817.1:p.Val36Met
XM_024448050.1:c.106G>A	XP_024303818.1:p.Val36Met
XM_024448051.1:c.106G>A	XP_024303819.1:p.Val36Met
XM_024448052.1:c.106G>A	XP_024303820.1:p.Val36Met
XM_024448053.1:c.106G>A	XP_024303821.1:p.Val36Met
XM_024448054.1:c.106G>A	XP_024303822.1:p.Val36Met
XR_002957065.1:n.171-31C>T
NM_001290020.2:c.106G>A	NP_001276949.1:p.Val36Met
NM_018076.5:c.106G>A MANE Select	NP_060546.2:p.Val36Met