Canonical Allele Identifier: CA2619258817

Gene: RPS26

Linked Data

• gnomAD v4: 12-56041939-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041942del , CM000674.2:g.56041942del	GRCh38
NC_000012.11:g.56435726del , CM000674.1:g.56435726del	GRCh37
NC_000012.10:g.54721993del	NCBI36
NG_023201.1:g.5041del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-225del	ENSP00000348849.5:n.-225del
ENST00000646449.2:c.-225del MANE Select	ENSP00000496643.1:n.-225del
ENST00000356464.9:c.-225del	ENSP00000348849.5:n.-225del
ENST00000552361.1:c.-157del	ENSP00000450339.1:n.-157del
NM_001029.3:c.-225del	NP_001020.2:n.-225del
NM_001029.5:c.-225del MANE Select	NP_001020.2:n.-225del
XR_944989.3:n.64del
XR_944990.3:n.64del