Canonical Allele Identifier: CA935656792

Gene: CSRP3

Linked Data

• dbSNP Id: rs1850568354
• gnomAD v3: 11-19188611-GAA-G
• gnomAD v4: 11-19188611-GAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188612_19188613del , CM000673.2:g.19188612_19188613del	GRCh38
NC_000011.9:g.19210159_19210160del , CM000673.1:g.19210159_19210160del	GRCh37
NC_000011.8:g.19166735_19166736del	NCBI36
NG_011932.2:g.26961_26962del , LRG_440:g.26961_26962del

Transcript Alleles

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