Canonical Allele Identifier: CA341769076
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115732968T>A , CM000663.2:g.115732968T>A GRCh38
NC_000001.10:g.116275589T>A , CM000663.1:g.116275589T>A GRCh37
NC_000001.9:g.116077112T>A NCBI36
NG_008802.1:g.40838A>T , LRG_404:g.40838A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.263A>T ENSP00000518226.1:p.Lys88Met
ENST00000261448.6:c.539A>T MANE Select ENSP00000261448.5:p.Lys180Met
ENST00000261448.5:c.539A>T ENSP00000261448.5:p.Lys180Met
NM_001232.3:c.539A>T , LRG_404t1:c.539A>T NP_001223.2:p.Lys180Met
NM_001232.4:c.539A>T MANE Select NP_001223.2:p.Lys180Met