Canonical Allele Identifier: CA1190742478
Gene: CASQ2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.-50T= ENSP00000518226.1:n.-50T=
ENST00000261448.6:c.227T= MANE Select ENSP00000261448.5:p.Val76=
ENST00000261448.5:c.227T= ENSP00000261448.5:p.Val76=
NM_001232.3:c.227T= , LRG_404t1:c.227T= NP_001223.2:p.Val76=
NM_001232.4:c.227T= MANE Select NP_001223.2:p.Val76=