Canonical Allele Identifier: CA1955950850

Gene: CSRP3

Linked Data

• dbSNP Id: rs1850568477

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188613_19188614dup , CM000673.2:g.19188613_19188614dup	GRCh38
NC_000011.9:g.19210160_19210161dup , CM000673.1:g.19210160_19210161dup	GRCh37
NC_000011.8:g.19166736_19166737dup	NCBI36
NG_011932.2:g.26960_26961dup , LRG_440:g.26960_26961dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.113-310_113-309dup MANE Select	ENSP00000265968.3:n.113-310_113-309dup
ENST00000533783.2:c.113-310_113-309dup	ENSP00000431813.1:n.113-310_113-309dup
ENST00000647990.1:c.113-310_113-309dup	ENSP00000496798.1:n.113-310_113-309dup
ENST00000648719.1:c.113-3569_113-3568dup	ENSP00000497633.1:n.113-3569_113-3568dup
ENST00000649235.1:c.113-310_113-309dup	ENSP00000497388.1:n.113-310_113-309dup
ENST00000649842.1:c.113-2266_113-2265dup	ENSP00000497531.1:n.113-2266_113-2265dup
ENST00000265968.7:c.113-310_113-309dup	ENSP00000265968.3:n.113-310_113-309dup
ENST00000533783.1:c.113-310_113-309dup	ENSP00000431813.1:n.113-310_113-309dup
NM_003476.4:c.113-310_113-309dup	NP_003467.1:n.113-310_113-309dup
XM_024448698.1:c.113-2266_113-2265dup	XP_024304466.1:n.113-2266_113-2265dup
NM_001369404.1:c.113-2266_113-2265dup	NP_001356333.1:n.113-2266_113-2265dup
NM_003476.5:c.113-310_113-309dup MANE Select	NP_003467.1:n.113-310_113-309dup