Canonical Allele Identifier: CA1190742432
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768218T= , CM000663.2:g.115768218T= GRCh38
NC_000001.10:g.116310839T= , CM000663.1:g.116310839T= GRCh37
NC_000001.9:g.116112362T= NCBI36
NG_008802.1:g.5588A= , LRG_404:g.5588A=

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.-43+90A= ENSP00000518226.1:n.-43+90A=
ENST00000261448.6:c.234+90A= MANE Select ENSP00000261448.5:n.234+90A=
ENST00000261448.5:c.234+90A= ENSP00000261448.5:n.234+90A=
NM_001232.3:c.234+90A= , LRG_404t1:c.234+90A= NP_001223.2:n.234+90A=
NM_001232.4:c.234+90A= MANE Select NP_001223.2:n.234+90A=