Canonical Allele Identifier: CA2644080448

Gene: HMGCL

Linked Data

• gnomAD v4: 1-23817353-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23817353C>T , CM000663.2:g.23817353C>T	GRCh38
NC_000001.10:g.24143843C>T , CM000663.1:g.24143843C>T	GRCh37
NC_000001.9:g.24016430C>T	NCBI36
NG_013061.1:g.13107G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374490.8:c.252+123G>A MANE Select	ENSP00000363614.3:n.252+123G>A
ENST00000235958.4:c.131+3157G>A
ENST00000374487.6:c.*293+123G>A	ENSP00000363611.2:n.*293+123G>A
ENST00000374490.7:c.252+123G>A	ENSP00000363614.3:n.252+123G>A
ENST00000436439.6:c.252+123G>A	ENSP00000389281.2:n.252+123G>A
ENST00000498698.1:n.58+123G>A
ENST00000509389.5:n.264+123G>A
ENST00000513148.1:n.253+123G>A
NM_000191.2:c.252+123G>A	NP_000182.2:n.252+123G>A
NM_001166059.1:c.252+123G>A	NP_001159531.1:n.252+123G>A
NM_000191.3:c.252+123G>A MANE Select	NP_000182.2:n.252+123G>A
NM_001166059.2:c.252+123G>A	NP_001159531.1:n.252+123G>A