Canonical Allele Identifier: CA2647280132
Gene: CASQ2 HGNC NCBI

Linked Data

gnomAD v4: 1-115738434-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115738436del , CM000663.2:g.115738436del GRCh38
NC_000001.10:g.116281057del , CM000663.1:g.116281057del GRCh37
NC_000001.9:g.116082580del NCBI36
NG_008802.1:g.35371del , LRG_404:g.35371del

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.145-100del ENSP00000518226.1:n.145-100del
ENST00000261448.6:c.421-100del MANE Select ENSP00000261448.5:n.421-100del
ENST00000261448.5:c.421-100del ENSP00000261448.5:n.421-100del
NM_001232.3:c.421-100del , LRG_404t1:c.421-100del NP_001223.2:n.421-100del
NM_001232.4:c.421-100del MANE Select NP_001223.2:n.421-100del
Search 100 bp 5'
Search 100 bp 3'