Canonical Allele Identifier: CA341766996
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768325T>G , CM000663.2:g.115768325T>G GRCh38
NC_000001.10:g.116310946T>G , CM000663.1:g.116310946T>G GRCh37
NC_000001.9:g.116112469T>G NCBI36
NG_008802.1:g.5481A>C , LRG_404:g.5481A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-60A>C ENSP00000518226.1:n.-60A>C
ENST00000261448.6:c.217A>C MANE Select ENSP00000261448.5:p.Lys73Gln
ENST00000261448.5:c.217A>C ENSP00000261448.5:p.Lys73Gln
NM_001232.3:c.217A>C , LRG_404t1:c.217A>C NP_001223.2:p.Lys73Gln
NM_001232.4:c.217A>C MANE Select NP_001223.2:p.Lys73Gln