Canonical Allele Identifier: CA1143852368
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115738277C= , CM000663.2:g.115738277C= GRCh38
NC_000001.10:g.116280898C= , CM000663.1:g.116280898C= GRCh37
NC_000001.9:g.116082421C= NCBI36
NG_008802.1:g.35529G= , LRG_404:g.35529G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.203G= ENSP00000518226.1:p.Arg68=
ENST00000261448.6:c.479G= MANE Select ENSP00000261448.5:p.Arg160=
ENST00000261448.5:c.479G= ENSP00000261448.5:p.Arg160=
NM_001232.3:c.479G= , LRG_404t1:c.479G= NP_001223.2:p.Arg160=
NM_001232.4:c.479G= MANE Select NP_001223.2:p.Arg160=