Canonical Allele Identifier: CA309294196

Gene: ODAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48297670T>C , CM000681.2:g.48297670T>C	GRCh38
NC_000019.9:g.48800927T>C , CM000681.1:g.48800927T>C	GRCh37
NC_000019.8:g.53492739T>C	NCBI36
NG_033251.1:g.27406A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001364171.2:c.1503-2A>G MANE Select	NP_001351100.1:n.1503-2A>G
ENST00000674294.1:c.1503-2A>G MANE Select	ENSP00000501363.1:n.1503-2A>G
NM_001364171.1:c.1503-2A>G	NP_001351100.1:n.1503-2A>G
NM_144577.3:c.1392-2A>G	NP_653178.3:n.1392-2A>G
NM_144577.4:c.1392-2A>G	NP_653178.3:n.1392-2A>G
ENST00000315396.7:c.1392-2A>G	ENSP00000318429.7:n.1392-2A>G
ENST00000474199.5:n.1520-2A>G
ENST00000474199.6:c.1503-2A>G	ENSP00000501357.1:n.1503-2A>G
ENST00000497273.1:n.938-2A>G
ENST00000674207.1:c.*1113-7A>G	ENSP00000501374.1:n.*1113-7A>G
XM_005259413.2:c.1503-2A>G	XP_005259470.1:n.1503-2A>G
XM_005259414.2:c.1503-2A>G	XP_005259471.1:n.1503-2A>G
XM_005259414.3:c.1503-2A>G	XP_005259471.1:n.1503-2A>G
XM_005259415.2:c.1503-2A>G	XP_005259472.1:n.1503-2A>G
XM_005259415.3:c.1503-2A>G	XP_005259472.1:n.1503-2A>G
XM_005259416.3:c.819-2A>G	XP_005259473.1:n.819-2A>G
XM_005259416.4:c.819-2A>G	XP_005259473.1:n.819-2A>G
XM_011527515.1:c.1392-2A>G	XP_011525817.1:n.1392-2A>G
XM_011527515.2:c.1392-2A>G	XP_011525817.1:n.1392-2A>G
XM_011527516.1:c.1392-2A>G	XP_011525818.1:n.1392-2A>G
XM_011527516.2:c.1392-2A>G	XP_011525818.1:n.1392-2A>G
XM_017027483.1:c.1227-2A>G	XP_016882972.1:n.1227-2A>G
XM_024451782.1:c.1542-2A>G	XP_024307550.1:n.1542-2A>G
XM_024451783.1:c.1503-2A>G	XP_024307551.1:n.1503-2A>G