Canonical Allele Identifier: CA204531663

Gene: ODAD2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27981583C>T , CM000672.2:g.27981583C>T	GRCh38
NC_000010.10:g.28270512C>T , CM000672.1:g.28270512C>T	GRCh37
NC_000010.9:g.28310518C>T	NCBI36
NG_042820.1:g.22468G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018076.5:c.820-1G>A MANE Select	NP_060546.2:n.820-1G>A
ENST00000305242.10:c.820-1G>A MANE Select	ENSP00000306410.5:n.820-1G>A
NM_001290020.1:c.820-1G>A	NP_001276949.1:n.820-1G>A
NM_001290020.2:c.820-1G>A	NP_001276949.1:n.820-1G>A
NM_001290021.1:c.-304-1G>A	NP_001276950.1:n.-304-1G>A
NM_001290021.2:c.-304-1G>A	NP_001276950.1:n.-304-1G>A
NM_001312689.1:c.-105-1G>A	NP_001299618.1:n.-105-1G>A
NM_001312689.2:c.-105-1G>A	NP_001299618.1:n.-105-1G>A
NM_018076.3:c.820-1G>A	NP_060546.2:n.820-1G>A
NM_018076.4:c.820-1G>A	NP_060546.2:n.820-1G>A
ENST00000305242.9:c.820-1G>A	ENSP00000306410.5:n.820-1G>A
ENST00000434029.1:c.502-1G>A	ENSP00000398155.1:n.502-1G>A
ENST00000480504.1:n.77-1G>A
ENST00000672841.1:c.-105-1G>A	ENSP00000499983.1:n.-105-1G>A
ENST00000672877.1:c.-304-1G>A	ENSP00000500120.1:n.-304-1G>A
ENST00000673384.1:c.-105-1G>A	ENSP00000500856.1:n.-105-1G>A
ENST00000673439.1:c.820-1G>A	ENSP00000500782.1:n.820-1G>A
ENST00000673512.1:c.-106G>A	ENSP00000499923.1:n.-106G>A
XM_011519526.1:c.820-1G>A	XP_011517828.1:n.820-1G>A
XM_011519527.1:c.820-1G>A	XP_011517829.1:n.820-1G>A
XM_011519528.1:c.820-1G>A	XP_011517830.1:n.820-1G>A
XM_011519529.1:c.820-1G>A	XP_011517831.1:n.820-1G>A
XM_011519530.1:c.820-1G>A	XP_011517832.1:n.820-1G>A
XM_011519531.1:c.820-1G>A	XP_011517833.1:n.820-1G>A
XM_011519532.1:c.820-1G>A	XP_011517834.1:n.820-1G>A
XM_011519533.1:c.-105-1G>A	XP_011517835.1:n.-105-1G>A
XM_011519534.1:c.-105-1G>A	XP_011517836.1:n.-105-1G>A
XM_011519535.1:c.-151+1346G>A	XP_011517837.1:n.-151+1346G>A
XM_011519536.1:c.820-1G>A	XP_011517838.1:n.820-1G>A
XM_017016371.1:c.820-1G>A	XP_016871860.1:n.820-1G>A
XM_024448049.1:c.820-1G>A	XP_024303817.1:n.820-1G>A
XM_024448050.1:c.820-1G>A	XP_024303818.1:n.820-1G>A
XM_024448051.1:c.820-1G>A	XP_024303819.1:n.820-1G>A
XM_024448052.1:c.820-1G>A	XP_024303820.1:n.820-1G>A
XM_024448053.1:c.820-1G>A	XP_024303821.1:n.820-1G>A
XM_024448054.1:c.820-1G>A	XP_024303822.1:n.820-1G>A
XM_024448055.1:c.-105-1G>A	XP_024303823.1:n.-105-1G>A
XM_024448056.1:c.-105-1G>A	XP_024303824.1:n.-105-1G>A
XM_024448057.1:c.-151+1346G>A	XP_024303825.1:n.-151+1346G>A