Canonical Allele Identifier: CA2535475156

Gene: CSRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188624_19188625insCG , CM000673.2:g.19188624_19188625insCG	GRCh38
NC_000011.9:g.19210171_19210172insCG , CM000673.1:g.19210171_19210172insCG	GRCh37
NC_000011.8:g.19166747_19166748insCG	NCBI36
NG_011932.2:g.26950_26951insGC , LRG_440:g.26950_26951insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.113-320_113-319insGC MANE Select	ENSP00000265968.3:n.113-320_113-319insGC
ENST00000533783.2:c.113-320_113-319insGC	ENSP00000431813.1:n.113-320_113-319insGC
ENST00000647990.1:c.113-320_113-319insGC	ENSP00000496798.1:n.113-320_113-319insGC
ENST00000648719.1:c.113-3579_113-3578insGC	ENSP00000497633.1:n.113-3579_113-3578insGC
ENST00000649235.1:c.113-320_113-319insGC	ENSP00000497388.1:n.113-320_113-319insGC
ENST00000649842.1:c.113-2276_113-2275insGC	ENSP00000497531.1:n.113-2276_113-2275insGC
ENST00000265968.7:c.113-320_113-319insGC	ENSP00000265968.3:n.113-320_113-319insGC
ENST00000533783.1:c.113-320_113-319insGC	ENSP00000431813.1:n.113-320_113-319insGC
NM_003476.4:c.113-320_113-319insGC	NP_003467.1:n.113-320_113-319insGC
XM_024448698.1:c.113-2276_113-2275insGC	XP_024304466.1:n.113-2276_113-2275insGC
NM_001369404.1:c.113-2276_113-2275insGC	NP_001356333.1:n.113-2276_113-2275insGC
NM_003476.5:c.113-320_113-319insGC MANE Select	NP_003467.1:n.113-320_113-319insGC