Canonical Allele Identifier: CA2790639598

Gene: CSRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188622_19188623insGGTGTG , CM000673.2:g.19188622_19188623insGGTGTG	GRCh38
NC_000011.9:g.19210169_19210170insGGTGTG , CM000673.1:g.19210169_19210170insGGTGTG	GRCh37
NC_000011.8:g.19166745_19166746insGGTGTG	NCBI36
NG_011932.2:g.26956_26957insCCACAC , LRG_440:g.26956_26957insCCACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.113-314_113-313insCCACAC MANE Select	ENSP00000265968.3:n.113-314_113-313insCCACAC
ENST00000533783.2:c.113-314_113-313insCCACAC	ENSP00000431813.1:n.113-314_113-313insCCACAC
ENST00000647990.1:c.113-314_113-313insCCACAC	ENSP00000496798.1:n.113-314_113-313insCCACAC
ENST00000648719.1:c.113-3573_113-3572insCCACAC	ENSP00000497633.1:n.113-3573_113-3572insCCACAC
ENST00000649235.1:c.113-314_113-313insCCACAC	ENSP00000497388.1:n.113-314_113-313insCCACAC
ENST00000649842.1:c.113-2270_113-2269insCCACAC	ENSP00000497531.1:n.113-2270_113-2269insCCACAC
ENST00000265968.7:c.113-314_113-313insCCACAC	ENSP00000265968.3:n.113-314_113-313insCCACAC
ENST00000533783.1:c.113-314_113-313insCCACAC	ENSP00000431813.1:n.113-314_113-313insCCACAC
NM_003476.4:c.113-314_113-313insCCACAC	NP_003467.1:n.113-314_113-313insCCACAC
XM_024448698.1:c.113-2270_113-2269insCCACAC	XP_024304466.1:n.113-2270_113-2269insCCACAC
NM_001369404.1:c.113-2270_113-2269insCCACAC	NP_001356333.1:n.113-2270_113-2269insCCACAC
NM_003476.5:c.113-314_113-313insCCACAC MANE Select	NP_003467.1:n.113-314_113-313insCCACAC