Canonical Allele Identifier: CA13549162
Gene: CAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34446099A>G , CM000673.2:g.34446099A>G GRCh38
NC_000011.9:g.34467646A>G , CM000673.1:g.34467646A>G GRCh37
NC_000011.8:g.34424222A>G NCBI36
NG_013339.1:g.12175A>G
NG_013339.2:g.12175A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000241052.5:c.67-3093A>G MANE Select ENSP00000241052.4:n.67-3093A>G
ENST00000241052.4:c.67-3093A>G ENSP00000241052.4:n.67-3093A>G
NM_001752.3:c.67-3093A>G NP_001743.1:n.67-3093A>G
NM_001752.4:c.67-3093A>G MANE Select NP_001743.1:n.67-3093A>G