Canonical Allele Identifier: CA339023131

Gene: HMGCL

Linked Data

• MyVariant Identifiers: chr1:g.24134638A>G (hg19) ; chr1:g.23808148A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23808148A>G , CM000663.2:g.23808148A>G	GRCh38
NC_000001.10:g.24134638A>G , CM000663.1:g.24134638A>G	GRCh37
NC_000001.9:g.24007225A>G	NCBI36
NG_013061.1:g.22312T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374490.8:c.737T>C MANE Select	ENSP00000363614.3:p.Leu246Ser
ENST00000235958.4:c.307T>C
ENST00000374487.6:c.*778T>C	ENSP00000363611.2:n.*778T>C
ENST00000374490.7:c.737T>C	ENSP00000363614.3:p.Leu246Ser
ENST00000436439.6:c.524T>C	ENSP00000389281.2:p.Leu175Ser
ENST00000496907.1:n.372T>C
ENST00000509389.5:n.428T>C
NM_000191.2:c.737T>C	NP_000182.2:p.Leu246Ser
NM_001166059.1:c.524T>C	NP_001159531.1:p.Leu175Ser
NM_000191.3:c.737T>C MANE Select	NP_000182.2:p.Leu246Ser
NM_001166059.2:c.524T>C	NP_001159531.1:p.Leu175Ser