Canonical Allele Identifier: CA2612792917

Gene: CSRP3

Linked Data

• gnomAD v4: 11-19188195-TCCATA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188198_19188202del , CM000673.2:g.19188198_19188202del	GRCh38
NC_000011.9:g.19209745_19209749del , CM000673.1:g.19209745_19209749del	GRCh37
NC_000011.8:g.19166321_19166325del	NCBI36
NG_011932.2:g.27374_27378del , LRG_440:g.27374_27378del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265968.9:c.217_221del MANE Select	ENSP00000265968.3:p.Tyr73ThrfsTer?
ENST00000533783.2:c.217_221del	ENSP00000431813.1:p.Tyr73ThrfsTer?
ENST00000647990.1:c.217_221del	ENSP00000496798.1:p.Tyr73ThrfsTer?
ENST00000648719.1:c.113-3155_113-3151del	ENSP00000497633.1:n.113-3155_113-3151del
ENST00000649235.1:c.217_221del	ENSP00000497388.1:p.Tyr73ThrfsTer?
ENST00000649842.1:c.113-1852_113-1848del	ENSP00000497531.1:n.113-1852_113-1848del
ENST00000265968.7:c.217_221del	ENSP00000265968.3:p.Tyr73ThrfsTer?
ENST00000533783.1:c.217_221del	ENSP00000431813.1:p.Tyr73ThrfsTer?
NM_003476.4:c.217_221del	NP_003467.1:p.Tyr73ThrfsTer?
XM_024448698.1:c.113-1852_113-1848del	XP_024304466.1:n.113-1852_113-1848del
NM_001369404.1:c.113-1852_113-1848del	NP_001356333.1:n.113-1852_113-1848del
NM_003476.5:c.217_221del MANE Select	NP_003467.1:p.Tyr73ThrfsTer?