Canonical Allele Identifier: CA7453688

Gene: OTUD7A

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.31501727A>C , CM000677.2:g.31501727A>C	GRCh38
NC_000015.9:g.31793930A>C , CM000677.1:g.31793930A>C	GRCh37
NC_000015.8:g.29581222A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307050.6:c.1134T>G MANE Select	ENSP00000305926.5:p.Leu378=
ENST00000560598.2:c.1113T>G	ENSP00000453883.2:p.Leu371=
ENST00000678495.1:c.1113T>G	ENSP00000503326.1:p.Leu371=
ENST00000307050.5:c.1113T>G	ENSP00000305926.4:p.Leu371=
NM_130901.1:c.1113T>G	NP_570971.1:p.Leu371=
XM_011521287.1:c.1395T>G	XP_011519589.1:p.Leu465=
NM_001329907.1:c.1134T>G	NP_001316836.1:p.Leu378=
NM_130901.2:c.1113T>G	NP_570971.1:p.Leu371=
NM_001329907.2:c.1134T>G	NP_001316836.1:p.Leu378=
NM_130901.3:c.1113T>G	NP_570971.1:p.Leu371=
NM_001382637.1:c.1134T>G MANE Select	NP_001369566.1:p.Leu378=