Canonical Allele Identifier: CA1190726084
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115730994A= , CM000663.2:g.115730994A= GRCh38
NC_000001.10:g.116273615A= , CM000663.1:g.116273615A= GRCh37
NC_000001.9:g.116075138A= NCBI36
NG_008802.1:g.42812T= , LRG_404:g.42812T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.425+1120T= ENSP00000518226.1:n.425+1120T=
ENST00000261448.6:c.606+1907T= MANE Select ENSP00000261448.5:n.606+1907T=
ENST00000261448.5:c.606+1907T= ENSP00000261448.5:n.606+1907T=
ENST00000488931.1:n.122+1120T=
NM_001232.3:c.606+1907T= , LRG_404t1:c.606+1907T= NP_001223.2:n.606+1907T=
NM_001232.4:c.606+1907T= MANE Select NP_001223.2:n.606+1907T=