Canonical Allele Identifier: CA505749519

Gene: ODAD3

Linked Data

• dbSNP Id: rs1335378353
• gnomAD v2: 19-11533491-G-A
• gnomAD v4: 19-11422823-G-A
• MyVariant Identifiers: chr19:g.11533491G>A (hg19) ; chr19:g.11422823G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11422823G>A , CM000681.2:g.11422823G>A	GRCh38
NC_000019.9:g.11533491G>A , CM000681.1:g.11533491G>A	GRCh37
NC_000019.8:g.11394491G>A	NCBI36
NG_041777.1:g.17960C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.1155C>T MANE Select	ENSP00000348757.3:p.Phe385=
ENST00000356392.8:c.1155C>T	ENSP00000348757.3:p.Phe385=
ENST00000586836.5:c.582C>T	ENSP00000467429.1:p.Phe194=
ENST00000591179.5:c.975C>T	ENSP00000466800.1:p.Phe325=
ENST00000591345.5:c.*1074C>T	ENSP00000467313.1:n.*1074C>T
NM_001302453.1:c.993C>T	NP_001289382.1:p.Phe331=
NM_001302454.1:c.975C>T	NP_001289383.1:p.Phe325=
NM_145045.4:c.1155C>T	NP_659482.3:p.Phe385=
XM_017026241.1:c.*49C>T	XP_016881730.1:n.*49C>T
NM_145045.5:c.1155C>T MANE Select	NP_659482.3:p.Phe385=
NM_001302454.2:c.975C>T	NP_001289383.1:p.Phe325=