Canonical Allele Identifier: CA406082323

Gene: ZNF526 GSK3A

Linked Data

• MyVariant Identifiers: chr19:g.42730536G>C (hg19) ; chr19:g.42226384G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.42226384G>C , CM000681.2:g.42226384G>C	GRCh38
NC_000019.9:g.42730536G>C , CM000681.1:g.42730536G>C	GRCh37
NC_000019.8:g.47422376G>C	NCBI36
NG_053183.1:g.11114G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710326.1:c.1981G>C (ZNF526)	ENSP00000518206.1:p.Gly661Arg
ENST00000301215.8:c.1981G>C (ZNF526) MANE Select	ENSP00000301215.2:p.Gly661Arg
ENST00000677025.1:c.131C>G (GSK3A)
ENST00000678490.1:c.93+5673C>G
ENST00000301215.7:c.1981G>C (ZNF526)	ENSP00000301215.2:p.Gly661Arg
NM_001314033.1:c.1981G>C (ZNF526)	NP_001300962.1:p.Gly661Arg
NM_133444.1:c.1981G>C (ZNF526)	NP_597701.1:p.Gly661Arg
NM_133444.2:c.1981G>C (ZNF526)	NP_597701.1:p.Gly661Arg
NM_001314033.2:c.1981G>C (ZNF526)	NP_001300962.1:p.Gly661Arg
NM_001314033.3:c.1981G>C (ZNF526)	NP_001300962.1:p.Gly661Arg
NM_133444.3:c.1981G>C (ZNF526) MANE Select	NP_597701.1:p.Gly661Arg