Canonical Allele Identifier: CA339023088

Gene: HMGCL

Linked Data

• MyVariant Identifiers: chr1:g.24134633C>A (hg19) ; chr1:g.23808143C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23808143C>A , CM000663.2:g.23808143C>A	GRCh38
NC_000001.10:g.24134633C>A , CM000663.1:g.24134633C>A	GRCh37
NC_000001.9:g.24007220C>A	NCBI36
NG_013061.1:g.22317G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374490.8:c.742G>T MANE Select	ENSP00000363614.3:p.Ala248Ser
ENST00000235958.4:c.312G>T
ENST00000374487.6:c.*783G>T	ENSP00000363611.2:n.*783G>T
ENST00000374490.7:c.742G>T	ENSP00000363614.3:p.Ala248Ser
ENST00000436439.6:c.529G>T	ENSP00000389281.2:p.Ala177Ser
ENST00000496907.1:n.377G>T
ENST00000509389.5:n.433G>T
NM_000191.2:c.742G>T	NP_000182.2:p.Ala248Ser
NM_001166059.1:c.529G>T	NP_001159531.1:p.Ala177Ser
NM_000191.3:c.742G>T MANE Select	NP_000182.2:p.Ala248Ser
NM_001166059.2:c.529G>T	NP_001159531.1:p.Ala177Ser