Canonical Allele Identifier: CA1190726191
Gene: CASQ2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115731243A= , CM000663.2:g.115731243A= GRCh38
NC_000001.10:g.116273864A= , CM000663.1:g.116273864A= GRCh37
NC_000001.9:g.116075387A= NCBI36
NG_008802.1:g.42563T= , LRG_404:g.42563T=

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.425+871T= ENSP00000518226.1:n.425+871T=
ENST00000261448.6:c.606+1658T= MANE Select ENSP00000261448.5:n.606+1658T=
ENST00000261448.5:c.606+1658T= ENSP00000261448.5:n.606+1658T=
ENST00000488931.1:n.122+871T=
NM_001232.3:c.606+1658T= , LRG_404t1:c.606+1658T= NP_001223.2:n.606+1658T=
NM_001232.4:c.606+1658T= MANE Select NP_001223.2:n.606+1658T=
Search 100 bp 5'
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