Canonical Allele Identifier: CA1190742390
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768122C= , CM000663.2:g.115768122C= GRCh38
NC_000001.10:g.116310743C= , CM000663.1:g.116310743C= GRCh37
NC_000001.9:g.116112266C= NCBI36
NG_008802.1:g.5684G= , LRG_404:g.5684G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-43+186G= ENSP00000518226.1:n.-43+186G=
ENST00000261448.6:c.234+186G= MANE Select ENSP00000261448.5:n.234+186G=
ENST00000261448.5:c.234+186G= ENSP00000261448.5:n.234+186G=
NM_001232.3:c.234+186G= , LRG_404t1:c.234+186G= NP_001223.2:n.234+186G=
NM_001232.4:c.234+186G= MANE Select NP_001223.2:n.234+186G=