Canonical Allele Identifier: CA2647281192
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768235_115768236del , CM000663.2:g.115768235_115768236del GRCh38
NC_000001.10:g.116310856_116310857del , CM000663.1:g.116310856_116310857del GRCh37
NC_000001.9:g.116112379_116112380del NCBI36
NG_008802.1:g.5570_5571del , LRG_404:g.5570_5571del

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.-43+72_-43+73del ENSP00000518226.1:n.-43+72_-43+73del
ENST00000261448.6:c.234+72_234+73del MANE Select ENSP00000261448.5:n.234+72_234+73del
ENST00000261448.5:c.234+72_234+73del ENSP00000261448.5:n.234+72_234+73del
NM_001232.3:c.234+72_234+73del , LRG_404t1:c.234+72_234+73del NP_001223.2:n.234+72_234+73del
NM_001232.4:c.234+72_234+73del MANE Select NP_001223.2:n.234+72_234+73del