Canonical Allele Identifier: CA1158968203
Gene: HMGCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23817560T= , CM000663.2:g.23817560T= GRCh38
NC_000001.10:g.24144050T= , CM000663.1:g.24144050T= GRCh37
NC_000001.9:g.24016637T= NCBI36
NG_013061.1:g.12900A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374490.8:c.168A= MANE Select ENSP00000363614.3:p.Lys56=
ENST00000235958.4:c.131+2950A=
ENST00000374487.6:c.*209A= ENSP00000363611.2:n.*209A=
ENST00000374490.7:c.168A= ENSP00000363614.3:p.Lys56=
ENST00000436439.6:c.168A= ENSP00000389281.2:p.Lys56=
ENST00000509389.5:n.180A=
ENST00000513148.1:n.169A=
NM_000191.2:c.168A= NP_000182.2:p.Lys56=
NM_001166059.1:c.168A= NP_001159531.1:p.Lys56=
NM_000191.3:c.168A= MANE Select NP_000182.2:p.Lys56=
NM_001166059.2:c.168A= NP_001159531.1:p.Lys56=