Canonical Allele Identifier: CA1148878969
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768450T= , CM000663.2:g.115768450T= GRCh38
NC_000001.10:g.116311071T= , CM000663.1:g.116311071T= GRCh37
NC_000001.9:g.116112594T= NCBI36
NG_008802.1:g.5356A= , LRG_404:g.5356A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-185A= ENSP00000518226.1:n.-185A=
ENST00000261448.6:c.92A= MANE Select ENSP00000261448.5:p.Lys31=
ENST00000261448.5:c.92A= ENSP00000261448.5:p.Lys31=
NM_001232.3:c.92A= , LRG_404t1:c.92A= NP_001223.2:p.Lys31=
NM_001232.4:c.92A= MANE Select NP_001223.2:p.Lys31=