Canonical Allele Identifier: CA1190742476
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768312A= , CM000663.2:g.115768312A= GRCh38
NC_000001.10:g.116310933A= , CM000663.1:g.116310933A= GRCh37
NC_000001.9:g.116112456A= NCBI36
NG_008802.1:g.5494T= , LRG_404:g.5494T=

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.-47T= ENSP00000518226.1:n.-47T=
ENST00000261448.6:c.230T= MANE Select ENSP00000261448.5:p.Leu77=
ENST00000261448.5:c.230T= ENSP00000261448.5:p.Leu77=
NM_001232.3:c.230T= , LRG_404t1:c.230T= NP_001223.2:p.Leu77=
NM_001232.4:c.230T= MANE Select NP_001223.2:p.Leu77=