Canonical Allele Identifier: CA339024158

Gene: HMGCL

Linked Data

• MyVariant Identifiers: chr1:g.24134741C>A (hg19) ; chr1:g.23808251C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23808251C>A , CM000663.2:g.23808251C>A	GRCh38
NC_000001.10:g.24134741C>A , CM000663.1:g.24134741C>A	GRCh37
NC_000001.9:g.24007328C>A	NCBI36
NG_013061.1:g.22209G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374490.8:c.634G>T MANE Select	ENSP00000363614.3:p.Gly212Trp
ENST00000235958.4:c.204G>T
ENST00000374487.6:c.*675G>T	ENSP00000363611.2:n.*675G>T
ENST00000374490.7:c.634G>T	ENSP00000363614.3:p.Gly212Trp
ENST00000436439.6:c.421G>T	ENSP00000389281.2:p.Gly141Trp
ENST00000496907.1:n.269G>T
ENST00000509389.5:n.361-36G>T
NM_000191.2:c.634G>T	NP_000182.2:p.Gly212Trp
NM_001166059.1:c.421G>T	NP_001159531.1:p.Gly141Trp
NM_000191.3:c.634G>T MANE Select	NP_000182.2:p.Gly212Trp
NM_001166059.2:c.421G>T	NP_001159531.1:p.Gly141Trp