Canonical Allele Identifier: CA14075452

Gene: OTUD7A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.31537504C>T , CM000677.2:g.31537504C>T	GRCh38
NC_000015.9:g.31829707C>T , CM000677.1:g.31829707C>T	GRCh37
NC_000015.8:g.29616999C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307050.6:c.551-6696G>A MANE Select	ENSP00000305926.5:n.551-6696G>A
ENST00000560598.2:c.551-6696G>A	ENSP00000453883.2:n.551-6696G>A
ENST00000678495.1:c.551-6696G>A	ENSP00000503326.1:n.551-6696G>A
ENST00000307050.5:c.551-6696G>A	ENSP00000305926.4:n.551-6696G>A
NM_130901.1:c.551-6696G>A	NP_570971.1:n.551-6696G>A
XM_011521287.1:c.812-6696G>A	XP_011519589.1:n.812-6696G>A
NM_001329907.1:c.551-6696G>A	NP_001316836.1:n.551-6696G>A
NM_130901.2:c.551-6696G>A	NP_570971.1:n.551-6696G>A
NM_001329907.2:c.551-6696G>A	NP_001316836.1:n.551-6696G>A
NM_130901.3:c.551-6696G>A	NP_570971.1:n.551-6696G>A
NM_001382637.1:c.551-6696G>A MANE Select	NP_001369566.1:n.551-6696G>A