Canonical Allele Identifier: CA406664469

Gene: ODAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48311993C>T , CM000681.2:g.48311993C>T	GRCh38
NC_000019.9:g.48815250C>T , CM000681.1:g.48815250C>T	GRCh37
NC_000019.8:g.53507062C>T	NCBI36
NG_033251.1:g.13083G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001364171.2:c.483+1G>A MANE Select	NP_001351100.1:n.483+1G>A
ENST00000674294.1:c.483+1G>A MANE Select	ENSP00000501363.1:n.483+1G>A
NM_001364171.1:c.483+1G>A	NP_001351100.1:n.483+1G>A
NM_144577.3:c.372+1G>A	NP_653178.3:n.372+1G>A
NM_144577.4:c.372+1G>A	NP_653178.3:n.372+1G>A
ENST00000315396.7:c.372+1G>A	ENSP00000318429.7:n.372+1G>A
ENST00000474199.5:n.500+1G>A
ENST00000474199.6:c.483+1G>A	ENSP00000501357.1:n.483+1G>A
ENST00000504608.6:n.325-327G>A
ENST00000674207.1:c.*191+1G>A	ENSP00000501374.1:n.*191+1G>A
XM_005259413.2:c.483+1G>A	XP_005259470.1:n.483+1G>A
XM_005259414.2:c.483+1G>A	XP_005259471.1:n.483+1G>A
XM_005259414.3:c.483+1G>A	XP_005259471.1:n.483+1G>A
XM_005259415.2:c.483+1G>A	XP_005259472.1:n.483+1G>A
XM_005259415.3:c.483+1G>A	XP_005259472.1:n.483+1G>A
XM_011527515.1:c.372+1G>A	XP_011525817.1:n.372+1G>A
XM_011527515.2:c.372+1G>A	XP_011525817.1:n.372+1G>A
XM_011527516.1:c.372+1G>A	XP_011525818.1:n.372+1G>A
XM_011527516.2:c.372+1G>A	XP_011525818.1:n.372+1G>A
XM_011527517.1:c.483+1G>A	XP_011525819.1:n.483+1G>A
XM_011527518.1:c.483+1G>A	XP_011525820.1:n.483+1G>A
XM_017027483.1:c.207+1G>A	XP_016882972.1:n.207+1G>A
XM_024451782.1:c.522+1G>A	XP_024307550.1:n.522+1G>A
XM_024451783.1:c.483+1G>A	XP_024307551.1:n.483+1G>A