Canonical Allele Identifier: CA2644080472

Gene: HMGCL

Linked Data

• gnomAD v4: 1-23817387-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23817387C>A , CM000663.2:g.23817387C>A	GRCh38
NC_000001.10:g.24143877C>A , CM000663.1:g.24143877C>A	GRCh37
NC_000001.9:g.24016464C>A	NCBI36
NG_013061.1:g.13073G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374490.8:c.252+89G>T MANE Select	ENSP00000363614.3:n.252+89G>T
ENST00000235958.4:c.131+3123G>T
ENST00000374487.6:c.*293+89G>T	ENSP00000363611.2:n.*293+89G>T
ENST00000374490.7:c.252+89G>T	ENSP00000363614.3:n.252+89G>T
ENST00000436439.6:c.252+89G>T	ENSP00000389281.2:n.252+89G>T
ENST00000498698.1:n.58+89G>T
ENST00000509389.5:n.264+89G>T
ENST00000513148.1:n.253+89G>T
NM_000191.2:c.252+89G>T	NP_000182.2:n.252+89G>T
NM_001166059.1:c.252+89G>T	NP_001159531.1:n.252+89G>T
NM_000191.3:c.252+89G>T MANE Select	NP_000182.2:n.252+89G>T
NM_001166059.2:c.252+89G>T	NP_001159531.1:n.252+89G>T