Canonical Allele Identifier: CA2899841
Community Standard Title: NM_004181.5(UCHL1):c.-26C>T
Gene: UCHL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.41256951C>T , CM000666.2:g.41256951C>T GRCh38
NC_000004.11:g.41258968C>T , CM000666.1:g.41258968C>T GRCh37
NC_000004.10:g.40953725C>T NCBI36
NG_012931.1:g.5071C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004181.5:c.-26C>T MANE Select NP_004172.2:n.-26C>T
ENST00000284440.9:c.-26C>T MANE Select ENSP00000284440.4:n.-26C>T
NM_004181.4:c.-26C>T NP_004172.2:n.-26C>T
ENST00000284440.8:c.-26C>T ENSP00000284440.4:n.-26C>T
ENST00000381760.8:n.44C>T
ENST00000472501.5:n.6C>T
ENST00000503431.5:c.-26C>T ENSP00000422542.1:n.-26C>T
ENST00000504818.5:n.19C>T
ENST00000505232.5:c.-26C>T ENSP00000423348.1:n.-26C>T
ENST00000508768.5:c.-26C>T ENSP00000426895.1:n.-26C>T
ENST00000512419.5:c.-26C>T ENSP00000425714.1:n.-26C>T
ENST00000512788.1:c.-26C>T ENSP00000423623.1:n.-26C>T
ENST00000514924.5:c.-26C>T ENSP00000426634.1:n.-26C>T