Canonical Allele Identifier: CA9549058

Gene: ODAD1

Linked Data

• ClinVar Variation Id: 291254
• ClinVar RCV Id: RCV000360978 ; RCV001087518
• dbSNP Id: rs141961809
• ExAC: 19:48815383 A / G
• gnomAD v2: 19-48815383-A-G
• gnomAD v3: 19-48312126-A-G
• gnomAD v4: 19-48312126-A-G
• MyVariant Identifiers: chr19:g.48815383A>G (hg19) ; chr19:g.48312126A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48312126A>G , CM000681.2:g.48312126A>G	GRCh38
NC_000019.9:g.48815383A>G , CM000681.1:g.48815383A>G	GRCh37
NC_000019.8:g.53507195A>G	NCBI36
NG_033251.1:g.12950T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474199.6:c.361-10T>C	ENSP00000501357.1:n.361-10T>C
ENST00000674207.1:c.*69-10T>C	ENSP00000501374.1:n.*69-10T>C
ENST00000674294.1:c.361-10T>C MANE Select	ENSP00000501363.1:n.361-10T>C
ENST00000315396.7:c.250-10T>C	ENSP00000318429.7:n.250-10T>C
ENST00000474199.5:n.378-10T>C
ENST00000504608.6:n.325-460T>C
NM_144577.3:c.250-10T>C	NP_653178.3:n.250-10T>C
XM_005259413.2:c.361-10T>C	XP_005259470.1:n.361-10T>C
XM_005259414.2:c.361-10T>C	XP_005259471.1:n.361-10T>C
XM_005259415.2:c.361-10T>C	XP_005259472.1:n.361-10T>C
XM_011527515.1:c.250-10T>C	XP_011525817.1:n.250-10T>C
XM_011527516.1:c.250-10T>C	XP_011525818.1:n.250-10T>C
XM_011527517.1:c.361-10T>C	XP_011525819.1:n.361-10T>C
XM_011527518.1:c.361-10T>C	XP_011525820.1:n.361-10T>C
NM_001364171.1:c.361-10T>C	NP_001351100.1:n.361-10T>C
NM_144577.4:c.250-10T>C	NP_653178.3:n.250-10T>C
XM_005259414.3:c.361-10T>C	XP_005259471.1:n.361-10T>C
XM_005259415.3:c.361-10T>C	XP_005259472.1:n.361-10T>C
XM_011527515.2:c.250-10T>C	XP_011525817.1:n.250-10T>C
XM_011527516.2:c.250-10T>C	XP_011525818.1:n.250-10T>C
XM_017027483.1:c.85-10T>C	XP_016882972.1:n.85-10T>C
XM_024451782.1:c.400-10T>C	XP_024307550.1:n.400-10T>C
XM_024451783.1:c.361-10T>C	XP_024307551.1:n.361-10T>C
NM_001364171.2:c.361-10T>C MANE Select	NP_001351100.1:n.361-10T>C