Canonical Allele Identifier: CA1190726937
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115732968T= , CM000663.2:g.115732968T= GRCh38
NC_000001.10:g.116275589T= , CM000663.1:g.116275589T= GRCh37
NC_000001.9:g.116077112T= NCBI36
NG_008802.1:g.40838A= , LRG_404:g.40838A=

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.263A= ENSP00000518226.1:p.Lys88=
ENST00000261448.6:c.539A= MANE Select ENSP00000261448.5:p.Lys180=
ENST00000261448.5:c.539A= ENSP00000261448.5:p.Lys180=
NM_001232.3:c.539A= , LRG_404t1:c.539A= NP_001223.2:p.Lys180=
NM_001232.4:c.539A= MANE Select NP_001223.2:p.Lys180=