Canonical Allele Identifier: CA416624477

Gene: HMGCL

Linked Data

• MyVariant Identifiers: chr1:g.24144047G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23817557G>T , CM000663.2:g.23817557G>T	GRCh38
NC_000001.10:g.24144047G>T , CM000663.1:g.24144047G>T	GRCh37
NC_000001.9:g.24016634G>T	NCBI36
NG_013061.1:g.12903C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374490.8:c.171C>A MANE Select	ENSP00000363614.3:p.Ile57=
ENST00000235958.4:c.131+2953C>A
ENST00000374487.6:c.*212C>A	ENSP00000363611.2:n.*212C>A
ENST00000374490.7:c.171C>A	ENSP00000363614.3:p.Ile57=
ENST00000436439.6:c.171C>A	ENSP00000389281.2:p.Ile57=
ENST00000509389.5:n.183C>A
ENST00000513148.1:n.172C>A
NM_000191.2:c.171C>A	NP_000182.2:p.Ile57=
NM_001166059.1:c.171C>A	NP_001159531.1:p.Ile57=
NM_000191.3:c.171C>A MANE Select	NP_000182.2:p.Ile57=
NM_001166059.2:c.171C>A	NP_001159531.1:p.Ile57=