Canonical Allele Identifier: CA1190742544
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768519A= , CM000663.2:g.115768519A= GRCh38
NC_000001.10:g.116311140A= , CM000663.1:g.116311140A= GRCh37
NC_000001.9:g.116112663A= NCBI36
NG_008802.1:g.5287T= , LRG_404:g.5287T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-223-31T= ENSP00000518226.1:n.-223-31T=
ENST00000261448.6:c.23T= MANE Select ENSP00000261448.5:p.Ile8=
ENST00000261448.5:c.23T= ENSP00000261448.5:p.Ile8=
NM_001232.3:c.23T= , LRG_404t1:c.23T= NP_001223.2:p.Ile8=
NM_001232.4:c.23T= MANE Select NP_001223.2:p.Ile8=