Canonical Allele Identifier: CA658658032

Gene: CSRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19182692_19182694del , CM000673.2:g.19182692_19182694del	GRCh38
NC_000011.9:g.19204239_19204241del , CM000673.1:g.19204239_19204241del	GRCh37
NC_000011.8:g.19160815_19160817del	NCBI36
NG_011932.2:g.32884_32886del , LRG_440:g.32884_32886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.565_567del MANE Select	ENSP00000265968.3:p.Gln189del
ENST00000533783.2:c.565_567del	ENSP00000431813.1:p.Gln189del
ENST00000647990.1:c.432_434del	ENSP00000496798.1:p.Asn144del
ENST00000648719.1:c.*83_*85del	ENSP00000497633.1:n.*83_*85del
ENST00000649235.1:c.565_567del	ENSP00000497388.1:p.Gln189del
ENST00000649842.1:c.396_398del	ENSP00000497531.1:p.Asn132del
ENST00000265968.7:c.565_567del	ENSP00000265968.3:p.Gln189del
ENST00000533783.1:c.565_567del	ENSP00000431813.1:p.Gln189del
NM_003476.4:c.565_567del	NP_003467.1:p.Gln189del
XM_024448698.1:c.396_398del	XP_024304466.1:p.Asn132del
NM_001369404.1:c.396_398del	NP_001356333.1:p.Asn132del
NM_003476.5:c.565_567del MANE Select	NP_003467.1:p.Gln189del