Canonical Allele Identifier: CA1158968265
Gene: HMGCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23817596G= , CM000663.2:g.23817596G= GRCh38
NC_000001.10:g.24144086G= , CM000663.1:g.24144086G= GRCh37
NC_000001.9:g.24016673G= NCBI36
NG_013061.1:g.12864C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374490.8:c.145-13C= MANE Select ENSP00000363614.3:n.145-13C=
ENST00000235958.4:c.131+2914C=
ENST00000374487.6:c.*186-13C= ENSP00000363611.2:n.*186-13C=
ENST00000374490.7:c.145-13C= ENSP00000363614.3:n.145-13C=
ENST00000436439.6:c.145-13C= ENSP00000389281.2:n.145-13C=
ENST00000509389.5:n.157-13C=
ENST00000513148.1:n.146-13C=
NM_000191.2:c.145-13C= NP_000182.2:n.145-13C=
NM_001166059.1:c.145-13C= NP_001159531.1:n.145-13C=
NM_000191.3:c.145-13C= MANE Select NP_000182.2:n.145-13C=
NM_001166059.2:c.145-13C= NP_001159531.1:n.145-13C=