Canonical Allele Identifier: CA1190729269
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115738260T= , CM000663.2:g.115738260T= GRCh38
NC_000001.10:g.116280881T= , CM000663.1:g.116280881T= GRCh37
NC_000001.9:g.116082404T= NCBI36
NG_008802.1:g.35546A= , LRG_404:g.35546A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.220A= ENSP00000518226.1:p.Lys74=
ENST00000261448.6:c.496A= MANE Select ENSP00000261448.5:p.Lys166=
ENST00000261448.5:c.496A= ENSP00000261448.5:p.Lys166=
NM_001232.3:c.496A= , LRG_404t1:c.496A= NP_001223.2:p.Lys166=
NM_001232.4:c.496A= MANE Select NP_001223.2:p.Lys166=