Canonical Allele Identifier: CA341766970
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768313G>T , CM000663.2:g.115768313G>T GRCh38
NC_000001.10:g.116310934G>T , CM000663.1:g.116310934G>T GRCh37
NC_000001.9:g.116112457G>T NCBI36
NG_008802.1:g.5493C>A , LRG_404:g.5493C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.-48C>A ENSP00000518226.1:n.-48C>A
ENST00000261448.6:c.229C>A MANE Select ENSP00000261448.5:p.Leu77Ile
ENST00000261448.5:c.229C>A ENSP00000261448.5:p.Leu77Ile
NM_001232.3:c.229C>A , LRG_404t1:c.229C>A NP_001223.2:p.Leu77Ile
NM_001232.4:c.229C>A MANE Select NP_001223.2:p.Leu77Ile