Canonical Allele Identifier: CA339029347

Gene: HMGCL

Linked Data

• MyVariant Identifiers: chr1:g.24144050T>G (hg19) ; chr1:g.23817560T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23817560T>G , CM000663.2:g.23817560T>G	GRCh38
NC_000001.10:g.24144050T>G , CM000663.1:g.24144050T>G	GRCh37
NC_000001.9:g.24016637T>G	NCBI36
NG_013061.1:g.12900A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374490.8:c.168A>C MANE Select	ENSP00000363614.3:p.Lys56Asn
ENST00000235958.4:c.131+2950A>C
ENST00000374487.6:c.*209A>C	ENSP00000363611.2:n.*209A>C
ENST00000374490.7:c.168A>C	ENSP00000363614.3:p.Lys56Asn
ENST00000436439.6:c.168A>C	ENSP00000389281.2:p.Lys56Asn
ENST00000509389.5:n.180A>C
ENST00000513148.1:n.169A>C
NM_000191.2:c.168A>C	NP_000182.2:p.Lys56Asn
NM_001166059.1:c.168A>C	NP_001159531.1:p.Lys56Asn
NM_000191.3:c.168A>C MANE Select	NP_000182.2:p.Lys56Asn
NM_001166059.2:c.168A>C	NP_001159531.1:p.Lys56Asn