Canonical Allele Identifier: CA1023855

Gene: CASQ2

Linked Data

• dbSNP Id: rs1553194664
• ExAC: 1:116275512 A / G
• gnomAD v2: 1-116275512-A-G
• gnomAD v4: 1-115732891-A-G
• MyVariant Identifiers: chr1:g.116275512A>G (hg19) ; chr1:g.116275512_116275515delinsGGGT (hg19) ; chr1:g.115732891_115732894delinsGGGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115732891A>G , CM000663.2:g.115732891A>G	GRCh38
NC_000001.10:g.116275512A>G , CM000663.1:g.116275512A>G	GRCh37
NC_000001.9:g.116077035A>G	NCBI36
NG_008802.1:g.40915T>C , LRG_404:g.40915T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000488931.2:c.330+10T>C	ENSP00000518226.1:n.330+10T>C
ENST00000261448.6:c.606+10T>C MANE Select	ENSP00000261448.5:n.606+10T>C
ENST00000261448.5:c.606+10T>C	ENSP00000261448.5:n.606+10T>C
ENST00000488931.1:n.27+10T>C
NM_001232.3:c.606+10T>C , LRG_404t1:c.606+10T>C	NP_001223.2:n.606+10T>C
NM_001232.4:c.606+10T>C MANE Select	NP_001223.2:n.606+10T>C