Canonical Allele Identifier: CA341768931
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115732905T>A , CM000663.2:g.115732905T>A GRCh38
NC_000001.10:g.116275526T>A , CM000663.1:g.116275526T>A GRCh37
NC_000001.9:g.116077049T>A NCBI36
NG_008802.1:g.40901A>T , LRG_404:g.40901A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.326A>T ENSP00000518226.1:p.Lys109Ile
ENST00000261448.6:c.602A>T MANE Select ENSP00000261448.5:p.Lys201Ile
ENST00000261448.5:c.602A>T ENSP00000261448.5:p.Lys201Ile
ENST00000488931.1:n.23A>T
NM_001232.3:c.602A>T , LRG_404t1:c.602A>T NP_001223.2:p.Lys201Ile
NM_001232.4:c.602A>T MANE Select NP_001223.2:p.Lys201Ile