Canonical Allele Identifier: CA1190726933
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115732960C= , CM000663.2:g.115732960C= GRCh38
NC_000001.10:g.116275581C= , CM000663.1:g.116275581C= GRCh37
NC_000001.9:g.116077104C= NCBI36
NG_008802.1:g.40846G= , LRG_404:g.40846G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.271G= ENSP00000518226.1:p.Glu91=
ENST00000261448.6:c.547G= MANE Select ENSP00000261448.5:p.Glu183=
ENST00000261448.5:c.547G= ENSP00000261448.5:p.Glu183=
NM_001232.3:c.547G= , LRG_404t1:c.547G= NP_001223.2:p.Glu183=
NM_001232.4:c.547G= MANE Select NP_001223.2:p.Glu183=