Canonical Allele Identifier: CA2790639608

Gene: CSRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188620_19188621insGG , CM000673.2:g.19188620_19188621insGG	GRCh38
NC_000011.9:g.19210167_19210168insGG , CM000673.1:g.19210167_19210168insGG	GRCh37
NC_000011.8:g.19166743_19166744insGG	NCBI36
NG_011932.2:g.26954_26955insCC , LRG_440:g.26954_26955insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.113-316_113-315insCC MANE Select	ENSP00000265968.3:n.113-316_113-315insCC
ENST00000533783.2:c.113-316_113-315insCC	ENSP00000431813.1:n.113-316_113-315insCC
ENST00000647990.1:c.113-316_113-315insCC	ENSP00000496798.1:n.113-316_113-315insCC
ENST00000648719.1:c.113-3575_113-3574insCC	ENSP00000497633.1:n.113-3575_113-3574insCC
ENST00000649235.1:c.113-316_113-315insCC	ENSP00000497388.1:n.113-316_113-315insCC
ENST00000649842.1:c.113-2272_113-2271insCC	ENSP00000497531.1:n.113-2272_113-2271insCC
ENST00000265968.7:c.113-316_113-315insCC	ENSP00000265968.3:n.113-316_113-315insCC
ENST00000533783.1:c.113-316_113-315insCC	ENSP00000431813.1:n.113-316_113-315insCC
NM_003476.4:c.113-316_113-315insCC	NP_003467.1:n.113-316_113-315insCC
XM_024448698.1:c.113-2272_113-2271insCC	XP_024304466.1:n.113-2272_113-2271insCC
NM_001369404.1:c.113-2272_113-2271insCC	NP_001356333.1:n.113-2272_113-2271insCC
NM_003476.5:c.113-316_113-315insCC MANE Select	NP_003467.1:n.113-316_113-315insCC