Canonical Allele Identifier: CA2745154599
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115700703T>G , CM000663.2:g.115700703T>G GRCh38
NC_000001.10:g.116243324T>G , CM000663.1:g.116243324T>G GRCh37
NC_000001.9:g.116044847T>G NCBI36
NG_008802.1:g.73103A>C , LRG_404:g.73103A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.*1110A>C ENSP00000518226.1:n.*1110A>C
ENST00000261448.6:c.*538A>C MANE Select ENSP00000261448.5:n.*538A>C
ENST00000261448.5:c.*538A>C ENSP00000261448.5:n.*538A>C
NM_001232.3:c.*538A>C , LRG_404t1:c.*538A>C NP_001223.2:n.*538A>C
NM_001232.4:c.*538A>C MANE Select NP_001223.2:n.*538A>C