Canonical Allele Identifier: CA11874920
Gene: UCHL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41264029C>A , CM000666.2:g.41264029C>A GRCh38
NC_000004.11:g.41266046C>A , CM000666.1:g.41266046C>A GRCh37
NC_000004.10:g.40960803C>A NCBI36
NG_012931.1:g.12149C>A

Transcript Alleles

HGVS Amino-acid Change
NM_004181.5:c.527-74C>A MANE Select NP_004172.2:n.527-74C>A
ENST00000284440.9:c.527-74C>A MANE Select ENSP00000284440.4:n.527-74C>A
NM_004181.4:c.527-74C>A NP_004172.2:n.527-74C>A
ENST00000284440.8:c.527-74C>A ENSP00000284440.4:n.527-74C>A
ENST00000381760.8:n.1078-74C>A
ENST00000472501.5:n.1051-74C>A
ENST00000503431.5:c.527-74C>A ENSP00000422542.1:n.527-74C>A
ENST00000505232.5:c.*52-74C>A ENSP00000423348.1:n.*52-74C>A
ENST00000508768.5:c.479-74C>A ENSP00000426895.1:n.479-74C>A
ENST00000510566.1:n.178-74C>A
ENST00000512419.5:c.*316-74C>A ENSP00000425714.1:n.*316-74C>A
ENST00000512788.1:c.527-74C>A ENSP00000423623.1:n.527-74C>A
ENST00000514764.5:n.361-74C>A