Canonical Allele Identifier: CA339023365

Gene: HMGCL

Linked Data

• MyVariant Identifiers: chr1:g.24134666T>C (hg19) ; chr1:g.23808176T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23808176T>C , CM000663.2:g.23808176T>C	GRCh38
NC_000001.10:g.24134666T>C , CM000663.1:g.24134666T>C	GRCh37
NC_000001.9:g.24007253T>C	NCBI36
NG_013061.1:g.22284A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374490.8:c.709A>G MANE Select	ENSP00000363614.3:p.Thr237Ala
ENST00000235958.4:c.279A>G
ENST00000374487.6:c.*750A>G	ENSP00000363611.2:n.*750A>G
ENST00000374490.7:c.709A>G	ENSP00000363614.3:p.Thr237Ala
ENST00000436439.6:c.496A>G	ENSP00000389281.2:p.Thr166Ala
ENST00000496907.1:n.344A>G
ENST00000509389.5:n.400A>G
NM_000191.2:c.709A>G	NP_000182.2:p.Thr237Ala
NM_001166059.1:c.496A>G	NP_001159531.1:p.Thr166Ala
NM_000191.3:c.709A>G MANE Select	NP_000182.2:p.Thr237Ala
NM_001166059.2:c.496A>G	NP_001159531.1:p.Thr166Ala