Canonical Allele Identifier: CA2790639602

Gene: CSRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188619_19188620insCT , CM000673.2:g.19188619_19188620insCT	GRCh38
NC_000011.9:g.19210166_19210167insCT , CM000673.1:g.19210166_19210167insCT	GRCh37
NC_000011.8:g.19166742_19166743insCT	NCBI36
NG_011932.2:g.26955_26956insGA , LRG_440:g.26955_26956insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.113-315_113-314insGA MANE Select	ENSP00000265968.3:n.113-315_113-314insGA
ENST00000533783.2:c.113-315_113-314insGA	ENSP00000431813.1:n.113-315_113-314insGA
ENST00000647990.1:c.113-315_113-314insGA	ENSP00000496798.1:n.113-315_113-314insGA
ENST00000648719.1:c.113-3574_113-3573insGA	ENSP00000497633.1:n.113-3574_113-3573insGA
ENST00000649235.1:c.113-315_113-314insGA	ENSP00000497388.1:n.113-315_113-314insGA
ENST00000649842.1:c.113-2271_113-2270insGA	ENSP00000497531.1:n.113-2271_113-2270insGA
ENST00000265968.7:c.113-315_113-314insGA	ENSP00000265968.3:n.113-315_113-314insGA
ENST00000533783.1:c.113-315_113-314insGA	ENSP00000431813.1:n.113-315_113-314insGA
NM_003476.4:c.113-315_113-314insGA	NP_003467.1:n.113-315_113-314insGA
XM_024448698.1:c.113-2271_113-2270insGA	XP_024304466.1:n.113-2271_113-2270insGA
NM_001369404.1:c.113-2271_113-2270insGA	NP_001356333.1:n.113-2271_113-2270insGA
NM_003476.5:c.113-315_113-314insGA MANE Select	NP_003467.1:n.113-315_113-314insGA