Canonical Allele Identifier: CA1158970270
Gene: HMGCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23820442C= , CM000663.2:g.23820442C= GRCh38
NC_000001.10:g.24146932C= , CM000663.1:g.24146932C= GRCh37
NC_000001.9:g.24019519C= NCBI36
NG_013061.1:g.10018G=

Transcript Alleles

HGVS Amino-acid change
ENST00000374490.8:c.144+68G= MANE Select ENSP00000363614.3:n.144+68G=
ENST00000235958.4:c.131+68G=
ENST00000374487.6:c.*185+68G= ENSP00000363611.2:n.*185+68G=
ENST00000374490.7:c.144+68G= ENSP00000363614.3:n.144+68G=
ENST00000436439.6:c.144+68G= ENSP00000389281.2:n.144+68G=
ENST00000509389.5:n.156+68G=
ENST00000513148.1:n.145+68G=
NM_000191.2:c.144+68G= NP_000182.2:n.144+68G=
NM_001166059.1:c.144+68G= NP_001159531.1:n.144+68G=
NM_000191.3:c.144+68G= MANE Select NP_000182.2:n.144+68G=
NM_001166059.2:c.144+68G= NP_001159531.1:n.144+68G=