Canonical Allele Identifier: CA16616309

Gene: ODAD1

Linked Data

• ClinVar Variation Id: 406188
• ClinVar RCV Id: RCV000474496
• dbSNP Id: rs1060500990
• gnomAD v3: 19-48303645-C-T
• gnomAD v4: 19-48303645-C-T
• MyVariant Identifiers: chr19:g.48806902C>T (hg19) ; chr19:g.48303645C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48303645C>T , CM000681.2:g.48303645C>T	GRCh38
NC_000019.9:g.48806902C>T , CM000681.1:g.48806902C>T	GRCh37
NC_000019.8:g.53498714C>T	NCBI36
NG_033251.1:g.21431G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474199.6:c.988+5G>A	ENSP00000501357.1:n.988+5G>A
ENST00000674207.1:c.*696+5G>A	ENSP00000501374.1:n.*696+5G>A
ENST00000674294.1:c.988+5G>A MANE Select	ENSP00000501363.1:n.988+5G>A
ENST00000315396.7:c.877+5G>A	ENSP00000318429.7:n.877+5G>A
ENST00000474199.5:n.1005+5G>A
NM_144577.3:c.877+5G>A	NP_653178.3:n.877+5G>A
XM_005259413.2:c.988+5G>A	XP_005259470.1:n.988+5G>A
XM_005259414.2:c.988+5G>A	XP_005259471.1:n.988+5G>A
XM_005259415.2:c.988+5G>A	XP_005259472.1:n.988+5G>A
XM_005259416.3:c.304+5G>A	XP_005259473.1:n.304+5G>A
XM_011527515.1:c.877+5G>A	XP_011525817.1:n.877+5G>A
XM_011527516.1:c.877+5G>A	XP_011525818.1:n.877+5G>A
XM_011527517.1:c.988+5G>A	XP_011525819.1:n.988+5G>A
XM_011527518.1:c.988+5G>A	XP_011525820.1:n.988+5G>A
NM_001364171.1:c.988+5G>A	NP_001351100.1:n.988+5G>A
NM_144577.4:c.877+5G>A	NP_653178.3:n.877+5G>A
XM_005259414.3:c.988+5G>A	XP_005259471.1:n.988+5G>A
XM_005259415.3:c.988+5G>A	XP_005259472.1:n.988+5G>A
XM_005259416.4:c.304+5G>A	XP_005259473.1:n.304+5G>A
XM_011527515.2:c.877+5G>A	XP_011525817.1:n.877+5G>A
XM_011527516.2:c.877+5G>A	XP_011525818.1:n.877+5G>A
XM_017027483.1:c.712+5G>A	XP_016882972.1:n.712+5G>A
XM_024451782.1:c.1027+5G>A	XP_024307550.1:n.1027+5G>A
XM_024451783.1:c.988+5G>A	XP_024307551.1:n.988+5G>A
NM_001364171.2:c.988+5G>A MANE Select	NP_001351100.1:n.988+5G>A