Canonical Allele Identifier: CA339029302

Gene: HMGCL

Linked Data

• MyVariant Identifiers: chr1:g.24144042A>T (hg19) ; chr1:g.23817552A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23817552A>T , CM000663.2:g.23817552A>T	GRCh38
NC_000001.10:g.24144042A>T , CM000663.1:g.24144042A>T	GRCh37
NC_000001.9:g.24016629A>T	NCBI36
NG_013061.1:g.12908T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374490.8:c.176T>A MANE Select	ENSP00000363614.3:p.Leu59Gln
ENST00000235958.4:c.131+2958T>A
ENST00000374487.6:c.*217T>A	ENSP00000363611.2:n.*217T>A
ENST00000374490.7:c.176T>A	ENSP00000363614.3:p.Leu59Gln
ENST00000436439.6:c.176T>A	ENSP00000389281.2:p.Leu59Gln
ENST00000509389.5:n.188T>A
ENST00000513148.1:n.177T>A
NM_000191.2:c.176T>A	NP_000182.2:p.Leu59Gln
NM_001166059.1:c.176T>A	NP_001159531.1:p.Leu59Gln
NM_000191.3:c.176T>A MANE Select	NP_000182.2:p.Leu59Gln
NM_001166059.2:c.176T>A	NP_001159531.1:p.Leu59Gln