Canonical Allele Identifier: CA341769066
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115732962A>T , CM000663.2:g.115732962A>T GRCh38
NC_000001.10:g.116275583A>T , CM000663.1:g.116275583A>T GRCh37
NC_000001.9:g.116077106A>T NCBI36
NG_008802.1:g.40844T>A , LRG_404:g.40844T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.269T>A ENSP00000518226.1:p.Phe90Tyr
ENST00000261448.6:c.545T>A MANE Select ENSP00000261448.5:p.Phe182Tyr
ENST00000261448.5:c.545T>A ENSP00000261448.5:p.Phe182Tyr
NM_001232.3:c.545T>A , LRG_404t1:c.545T>A NP_001223.2:p.Phe182Tyr
NM_001232.4:c.545T>A MANE Select NP_001223.2:p.Phe182Tyr