Canonical Allele Identifier: CA1955950851

Gene: CSRP3

Linked Data

• dbSNP Id: rs1850568393

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188612_19188613insCG , CM000673.2:g.19188612_19188613insCG	GRCh38
NC_000011.9:g.19210159_19210160insCG , CM000673.1:g.19210159_19210160insCG	GRCh37
NC_000011.8:g.19166735_19166736insCG	NCBI36
NG_011932.2:g.26961_26962insCG , LRG_440:g.26961_26962insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.113-309_113-308insCG MANE Select	ENSP00000265968.3:n.113-309_113-308insCG
ENST00000533783.2:c.113-309_113-308insCG	ENSP00000431813.1:n.113-309_113-308insCG
ENST00000647990.1:c.113-309_113-308insCG	ENSP00000496798.1:n.113-309_113-308insCG
ENST00000648719.1:c.113-3568_113-3567insCG	ENSP00000497633.1:n.113-3568_113-3567insCG
ENST00000649235.1:c.113-309_113-308insCG	ENSP00000497388.1:n.113-309_113-308insCG
ENST00000649842.1:c.113-2265_113-2264insCG	ENSP00000497531.1:n.113-2265_113-2264insCG
ENST00000265968.7:c.113-309_113-308insCG	ENSP00000265968.3:n.113-309_113-308insCG
ENST00000533783.1:c.113-309_113-308insCG	ENSP00000431813.1:n.113-309_113-308insCG
NM_003476.4:c.113-309_113-308insCG	NP_003467.1:n.113-309_113-308insCG
XM_024448698.1:c.113-2265_113-2264insCG	XP_024304466.1:n.113-2265_113-2264insCG
NM_001369404.1:c.113-2265_113-2264insCG	NP_001356333.1:n.113-2265_113-2264insCG
NM_003476.5:c.113-309_113-308insCG MANE Select	NP_003467.1:n.113-309_113-308insCG