Canonical Allele Identifier: CA341769081
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115732970G>C , CM000663.2:g.115732970G>C GRCh38
NC_000001.10:g.116275591G>C , CM000663.1:g.116275591G>C GRCh37
NC_000001.9:g.116077114G>C NCBI36
NG_008802.1:g.40836C>G , LRG_404:g.40836C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.261C>G ENSP00000518226.1:p.Tyr87Ter
ENST00000261448.6:c.537C>G MANE Select ENSP00000261448.5:p.Tyr179Ter
ENST00000261448.5:c.537C>G ENSP00000261448.5:p.Tyr179Ter
NM_001232.3:c.537C>G , LRG_404t1:c.537C>G NP_001223.2:p.Tyr179Ter
NM_001232.4:c.537C>G MANE Select NP_001223.2:p.Tyr179Ter