Canonical Allele Identifier: CA341766992
Gene: CASQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768324T>A , CM000663.2:g.115768324T>A GRCh38
NC_000001.10:g.116310945T>A , CM000663.1:g.116310945T>A GRCh37
NC_000001.9:g.116112468T>A NCBI36
NG_008802.1:g.5482A>T , LRG_404:g.5482A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-59A>T ENSP00000518226.1:n.-59A>T
ENST00000261448.6:c.218A>T MANE Select ENSP00000261448.5:p.Lys73Ile
ENST00000261448.5:c.218A>T ENSP00000261448.5:p.Lys73Ile
NM_001232.3:c.218A>T , LRG_404t1:c.218A>T NP_001223.2:p.Lys73Ile
NM_001232.4:c.218A>T MANE Select NP_001223.2:p.Lys73Ile