Canonical Allele Identifier: CA674410225

Gene: CSRP3

Linked Data

• dbSNP Id: rs138192808
• gnomAD v3: 11-19188613-A-AGTGTGTGTGTGTGTGTGTGT
• gnomAD v4: 11-19188613-A-AGTGTGTGTGTGTGTGTGTGT
• MyVariant Identifiers: chr11:g.19210160_19210161insGTGTGTGTGTGTGTGTGTGT (hg19) ; chr11:g.19188613_19188614insGTGTGTGTGTGTGTGTGTGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188632_19188651dup , CM000673.2:g.19188632_19188651dup	GRCh38
NC_000011.9:g.19210179_19210198dup , CM000673.1:g.19210179_19210198dup	GRCh37
NC_000011.8:g.19166755_19166774dup	NCBI36
NG_011932.2:g.26941_26960dup , LRG_440:g.26941_26960dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.113-329_113-310dup MANE Select	ENSP00000265968.3:n.113-329_113-310dup
ENST00000533783.2:c.113-329_113-310dup	ENSP00000431813.1:n.113-329_113-310dup
ENST00000647990.1:c.113-329_113-310dup	ENSP00000496798.1:n.113-329_113-310dup
ENST00000648719.1:c.113-3588_113-3569dup	ENSP00000497633.1:n.113-3588_113-3569dup
ENST00000649235.1:c.113-329_113-310dup	ENSP00000497388.1:n.113-329_113-310dup
ENST00000649842.1:c.113-2285_113-2266dup	ENSP00000497531.1:n.113-2285_113-2266dup
ENST00000265968.7:c.113-329_113-310dup	ENSP00000265968.3:n.113-329_113-310dup
ENST00000533783.1:c.113-329_113-310dup	ENSP00000431813.1:n.113-329_113-310dup
NM_003476.4:c.113-329_113-310dup	NP_003467.1:n.113-329_113-310dup
XM_024448698.1:c.113-2285_113-2266dup	XP_024304466.1:n.113-2285_113-2266dup
NM_001369404.1:c.113-2285_113-2266dup	NP_001356333.1:n.113-2285_113-2266dup
NM_003476.5:c.113-329_113-310dup MANE Select	NP_003467.1:n.113-329_113-310dup