Canonical Allele Identifier: CA341769090
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115732973G>T , CM000663.2:g.115732973G>T GRCh38
NC_000001.10:g.116275594G>T , CM000663.1:g.116275594G>T GRCh37
NC_000001.9:g.116077117G>T NCBI36
NG_008802.1:g.40833C>A , LRG_404:g.40833C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.258C>A ENSP00000518226.1:p.Tyr86Ter
ENST00000261448.6:c.534C>A MANE Select ENSP00000261448.5:p.Tyr178Ter
ENST00000261448.5:c.534C>A ENSP00000261448.5:p.Tyr178Ter
NM_001232.3:c.534C>A , LRG_404t1:c.534C>A NP_001223.2:p.Tyr178Ter
NM_001232.4:c.534C>A MANE Select NP_001223.2:p.Tyr178Ter