Canonical Allele Identifier: CA420178464
Gene: CASQ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.116311106T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768485T>A , CM000663.2:g.115768485T>A GRCh38
NC_000001.10:g.116311106T>A , CM000663.1:g.116311106T>A GRCh37
NC_000001.9:g.116112629T>A NCBI36
NG_008802.1:g.5321A>T , LRG_404:g.5321A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-220A>T ENSP00000518226.1:n.-220A>T
ENST00000261448.6:c.57A>T MANE Select ENSP00000261448.5:p.Ala19=
ENST00000261448.5:c.57A>T ENSP00000261448.5:p.Ala19=
NM_001232.3:c.57A>T , LRG_404t1:c.57A>T NP_001223.2:p.Ala19=
NM_001232.4:c.57A>T MANE Select NP_001223.2:p.Ala19=
Search 100 bp 5'
Search 100 bp 3'