Canonical Allele Identifier: CA2742819878
Gene: HMGCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23817357del , CM000663.2:g.23817357del GRCh38
NC_000001.10:g.24143847del , CM000663.1:g.24143847del GRCh37
NC_000001.9:g.24016434del NCBI36
NG_013061.1:g.13103del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374490.8:c.252+119del MANE Select ENSP00000363614.3:n.252+119del
ENST00000235958.4:c.131+3153del
ENST00000374487.6:c.*293+119del ENSP00000363611.2:n.*293+119del
ENST00000374490.7:c.252+119del ENSP00000363614.3:n.252+119del
ENST00000436439.6:c.252+119del ENSP00000389281.2:n.252+119del
ENST00000498698.1:n.58+119del
ENST00000509389.5:n.264+119del
ENST00000513148.1:n.253+119del
NM_000191.2:c.252+119del NP_000182.2:n.252+119del
NM_001166059.1:c.252+119del NP_001159531.1:n.252+119del
NM_000191.3:c.252+119del MANE Select NP_000182.2:n.252+119del
NM_001166059.2:c.252+119del NP_001159531.1:n.252+119del