Canonical Allele Identifier: CA1190712932
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115705215T= , CM000663.2:g.115705215T= GRCh38
NC_000001.10:g.116247836T= , CM000663.1:g.116247836T= GRCh37
NC_000001.9:g.116049359T= NCBI36
NG_008802.1:g.68591A= , LRG_404:g.68591A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.*288A= ENSP00000518226.1:n.*288A=
ENST00000261448.6:c.916A= MANE Select ENSP00000261448.5:p.Ile306=
ENST00000261448.5:c.916A= ENSP00000261448.5:p.Ile306=
NM_001232.3:c.916A= , LRG_404t1:c.916A= NP_001223.2:p.Ile306=
NM_001232.4:c.916A= MANE Select NP_001223.2:p.Ile306=