Canonical Allele Identifier: CA341767195
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768412G>T , CM000663.2:g.115768412G>T GRCh38
NC_000001.10:g.116311033G>T , CM000663.1:g.116311033G>T GRCh37
NC_000001.9:g.116112556G>T NCBI36
NG_008802.1:g.5394C>A , LRG_404:g.5394C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-147C>A ENSP00000518226.1:n.-147C>A
ENST00000261448.6:c.130C>A MANE Select ENSP00000261448.5:p.Gln44Lys
ENST00000261448.5:c.130C>A ENSP00000261448.5:p.Gln44Lys
NM_001232.3:c.130C>A , LRG_404t1:c.130C>A NP_001223.2:p.Gln44Lys
NM_001232.4:c.130C>A MANE Select NP_001223.2:p.Gln44Lys