Canonical Allele Identifier: CA1190742564
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768556G= , CM000663.2:g.115768556G= GRCh38
NC_000001.10:g.116311177G= , CM000663.1:g.116311177G= GRCh37
NC_000001.9:g.116112700G= NCBI36
NG_008802.1:g.5250C= , LRG_404:g.5250C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-223-68C= ENSP00000518226.1:n.-223-68C=
ENST00000261448.6:c.-15C= MANE Select ENSP00000261448.5:n.-15C=
ENST00000261448.5:c.-15C= ENSP00000261448.5:n.-15C=
NM_001232.3:c.-15C= , LRG_404t1:c.-15C= NP_001223.2:n.-15C=
NM_001232.4:c.-15C= MANE Select NP_001223.2:n.-15C=