Canonical Allele Identifier: CA1190729276
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115738278G= , CM000663.2:g.115738278G= GRCh38
NC_000001.10:g.116280899G= , CM000663.1:g.116280899G= GRCh37
NC_000001.9:g.116082422G= NCBI36
NG_008802.1:g.35528C= , LRG_404:g.35528C=

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.202C= ENSP00000518226.1:p.Arg68=
ENST00000261448.6:c.478C= MANE Select ENSP00000261448.5:p.Arg160=
ENST00000261448.5:c.478C= ENSP00000261448.5:p.Arg160=
NM_001232.3:c.478C= , LRG_404t1:c.478C= NP_001223.2:p.Arg160=
NM_001232.4:c.478C= MANE Select NP_001223.2:p.Arg160=