Canonical Allele Identifier: CA339029175

Gene: HMGCL

Linked Data

• MyVariant Identifiers: chr1:g.24144018C>G (hg19) ; chr1:g.23817528C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23817528C>G , CM000663.2:g.23817528C>G	GRCh38
NC_000001.10:g.24144018C>G , CM000663.1:g.24144018C>G	GRCh37
NC_000001.9:g.24016605C>G	NCBI36
NG_013061.1:g.12932G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374490.8:c.200G>C MANE Select	ENSP00000363614.3:p.Gly67Ala
ENST00000235958.4:c.131+2982G>C
ENST00000374487.6:c.*241G>C	ENSP00000363611.2:n.*241G>C
ENST00000374490.7:c.200G>C	ENSP00000363614.3:p.Gly67Ala
ENST00000436439.6:c.200G>C	ENSP00000389281.2:p.Gly67Ala
ENST00000498698.1:n.6G>C
ENST00000509389.5:n.212G>C
ENST00000513148.1:n.201G>C
NM_000191.2:c.200G>C	NP_000182.2:p.Gly67Ala
NM_001166059.1:c.200G>C	NP_001159531.1:p.Gly67Ala
NM_000191.3:c.200G>C MANE Select	NP_000182.2:p.Gly67Ala
NM_001166059.2:c.200G>C	NP_001159531.1:p.Gly67Ala