Canonical Allele Identifier: CA2644078302

Gene: HMGCL

Linked Data

• gnomAD v4: 1-23820432-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23820432T>G , CM000663.2:g.23820432T>G	GRCh38
NC_000001.10:g.24146922T>G , CM000663.1:g.24146922T>G	GRCh37
NC_000001.9:g.24019509T>G	NCBI36
NG_013061.1:g.10028A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374490.8:c.144+78A>C MANE Select	ENSP00000363614.3:n.144+78A>C
ENST00000235958.4:c.131+78A>C
ENST00000374487.6:c.*185+78A>C	ENSP00000363611.2:n.*185+78A>C
ENST00000374490.7:c.144+78A>C	ENSP00000363614.3:n.144+78A>C
ENST00000436439.6:c.144+78A>C	ENSP00000389281.2:n.144+78A>C
ENST00000509389.5:n.156+78A>C
ENST00000513148.1:n.145+78A>C
NM_000191.2:c.144+78A>C	NP_000182.2:n.144+78A>C
NM_001166059.1:c.144+78A>C	NP_001159531.1:n.144+78A>C
NM_000191.3:c.144+78A>C MANE Select	NP_000182.2:n.144+78A>C
NM_001166059.2:c.144+78A>C	NP_001159531.1:n.144+78A>C