Canonical Allele Identifier: CA339029181

Gene: HMGCL

Linked Data

• MyVariant Identifiers: chr1:g.24144019C>G (hg19) ; chr1:g.23817529C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23817529C>G , CM000663.2:g.23817529C>G	GRCh38
NC_000001.10:g.24144019C>G , CM000663.1:g.24144019C>G	GRCh37
NC_000001.9:g.24016606C>G	NCBI36
NG_013061.1:g.12931G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374490.8:c.199G>C MANE Select	ENSP00000363614.3:p.Gly67Arg
ENST00000235958.4:c.131+2981G>C
ENST00000374487.6:c.*240G>C	ENSP00000363611.2:n.*240G>C
ENST00000374490.7:c.199G>C	ENSP00000363614.3:p.Gly67Arg
ENST00000436439.6:c.199G>C	ENSP00000389281.2:p.Gly67Arg
ENST00000498698.1:n.5G>C
ENST00000509389.5:n.211G>C
ENST00000513148.1:n.200G>C
NM_000191.2:c.199G>C	NP_000182.2:p.Gly67Arg
NM_001166059.1:c.199G>C	NP_001159531.1:p.Gly67Arg
NM_000191.3:c.199G>C MANE Select	NP_000182.2:p.Gly67Arg
NM_001166059.2:c.199G>C	NP_001159531.1:p.Gly67Arg