Canonical Allele Identifier: CA1190726037
Gene: CASQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115730858T= , CM000663.2:g.115730858T= GRCh38
NC_000001.10:g.116273479T= , CM000663.1:g.116273479T= GRCh37
NC_000001.9:g.116075002T= NCBI36
NG_008802.1:g.42948A= , LRG_404:g.42948A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.425+1256A= ENSP00000518226.1:n.425+1256A=
ENST00000261448.6:c.606+2043A= MANE Select ENSP00000261448.5:n.606+2043A=
ENST00000261448.5:c.606+2043A= ENSP00000261448.5:n.606+2043A=
ENST00000488931.1:n.122+1256A=
NM_001232.3:c.606+2043A= , LRG_404t1:c.606+2043A= NP_001223.2:n.606+2043A=
NM_001232.4:c.606+2043A= MANE Select NP_001223.2:n.606+2043A=