Canonical Allele Identifier: CA341766972
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768315A>T , CM000663.2:g.115768315A>T GRCh38
NC_000001.10:g.116310936A>T , CM000663.1:g.116310936A>T GRCh37
NC_000001.9:g.116112459A>T NCBI36
NG_008802.1:g.5491T>A , LRG_404:g.5491T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.-50T>A ENSP00000518226.1:n.-50T>A
ENST00000261448.6:c.227T>A MANE Select ENSP00000261448.5:p.Val76Glu
ENST00000261448.5:c.227T>A ENSP00000261448.5:p.Val76Glu
NM_001232.3:c.227T>A , LRG_404t1:c.227T>A NP_001223.2:p.Val76Glu
NM_001232.4:c.227T>A MANE Select NP_001223.2:p.Val76Glu