Canonical Allele Identifier: CA1190726936
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115732965_115732966delinsGC , CM000663.2:g.115732965_115732966delinsGC GRCh38
NC_000001.10:g.116275586_116275587delinsGC , CM000663.1:g.116275586_116275587delinsGC GRCh37
NC_000001.9:g.116077109_116077110delinsGC NCBI36
NG_008802.1:g.40840_40841delinsGC , LRG_404:g.40840_40841delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.265_266delinsGC ENSP00000518226.1:p.Ala89=
ENST00000261448.6:c.541_542delinsGC MANE Select ENSP00000261448.5:p.Ala181=
ENST00000261448.5:c.541_542delinsGC ENSP00000261448.5:p.Ala181=
NM_001232.3:c.541_542delinsGC , LRG_404t1:c.541_542delinsGC NP_001223.2:p.Ala181=
NM_001232.4:c.541_542delinsGC MANE Select NP_001223.2:p.Ala181=