Canonical Allele Identifier: CA416621186

Gene: HMGCL

Linked Data

• MyVariant Identifiers: chr1:g.24134682A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23808192A>C , CM000663.2:g.23808192A>C	GRCh38
NC_000001.10:g.24134682A>C , CM000663.1:g.24134682A>C	GRCh37
NC_000001.9:g.24007269A>C	NCBI36
NG_013061.1:g.22268T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374490.8:c.693T>G MANE Select	ENSP00000363614.3:p.Ala231=
ENST00000235958.4:c.263T>G
ENST00000374487.6:c.*734T>G	ENSP00000363611.2:n.*734T>G
ENST00000374490.7:c.693T>G	ENSP00000363614.3:p.Ala231=
ENST00000436439.6:c.480T>G	ENSP00000389281.2:p.Ala160=
ENST00000496907.1:n.328T>G
ENST00000509389.5:n.384T>G
NM_000191.2:c.693T>G	NP_000182.2:p.Ala231=
NM_001166059.1:c.480T>G	NP_001159531.1:p.Ala160=
NM_000191.3:c.693T>G MANE Select	NP_000182.2:p.Ala231=
NM_001166059.2:c.480T>G	NP_001159531.1:p.Ala160=