Canonical Allele Identifier: CA674410195

Gene: CSRP3

Linked Data

• dbSNP Id: rs138192808
• gnomAD v3: 11-19188613-AGTGTGTGTGTGT-A
• gnomAD v4: 11-19188613-AGTGTGTGTGTGT-A
• MyVariant Identifiers: chr11:g.19210161_19210172del (hg19) ; chr11:g.19188614_19188625del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188640_19188651del , CM000673.2:g.19188640_19188651del	GRCh38
NC_000011.9:g.19210187_19210198del , CM000673.1:g.19210187_19210198del	GRCh37
NC_000011.8:g.19166763_19166774del	NCBI36
NG_011932.2:g.26949_26960del , LRG_440:g.26949_26960del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.113-321_113-310del MANE Select	ENSP00000265968.3:n.113-321_113-310del
ENST00000533783.2:c.113-321_113-310del	ENSP00000431813.1:n.113-321_113-310del
ENST00000647990.1:c.113-321_113-310del	ENSP00000496798.1:n.113-321_113-310del
ENST00000648719.1:c.113-3580_113-3569del	ENSP00000497633.1:n.113-3580_113-3569del
ENST00000649235.1:c.113-321_113-310del	ENSP00000497388.1:n.113-321_113-310del
ENST00000649842.1:c.113-2277_113-2266del	ENSP00000497531.1:n.113-2277_113-2266del
ENST00000265968.7:c.113-321_113-310del	ENSP00000265968.3:n.113-321_113-310del
ENST00000533783.1:c.113-321_113-310del	ENSP00000431813.1:n.113-321_113-310del
NM_003476.4:c.113-321_113-310del	NP_003467.1:n.113-321_113-310del
XM_024448698.1:c.113-2277_113-2266del	XP_024304466.1:n.113-2277_113-2266del
NM_001369404.1:c.113-2277_113-2266del	NP_001356333.1:n.113-2277_113-2266del
NM_003476.5:c.113-321_113-310del MANE Select	NP_003467.1:n.113-321_113-310del