Canonical Allele Identifier: CA218633635
Gene: CSRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1309661
ClinVar RCV Id: RCV001754944
dbSNP Id: rs267606753
MyVariant Identifiers: chr11:g.19209800T>C (hg19) chr11:g.19188253T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188253T>C , CM000673.2:g.19188253T>C GRCh38
NC_000011.9:g.19209800T>C , CM000673.1:g.19209800T>C GRCh37
NC_000011.8:g.19166376T>C NCBI36
NG_011932.2:g.27321A>G , LRG_440:g.27321A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000265968.9:c.164A>G MANE Select ENSP00000265968.3:p.Glu55Gly
ENST00000533783.2:c.164A>G ENSP00000431813.1:p.Glu55Gly
ENST00000647990.1:c.164A>G ENSP00000496798.1:p.Glu55Gly
ENST00000648719.1:c.113-3208A>G ENSP00000497633.1:n.113-3208A>G
ENST00000649235.1:c.164A>G ENSP00000497388.1:p.Glu55Gly
ENST00000649842.1:c.113-1905A>G ENSP00000497531.1:n.113-1905A>G
ENST00000265968.7:c.164A>G ENSP00000265968.3:p.Glu55Gly
ENST00000533783.1:c.164A>G ENSP00000431813.1:p.Glu55Gly
NM_003476.4:c.164A>G NP_003467.1:p.Glu55Gly
XM_024448698.1:c.113-1905A>G XP_024304466.1:n.113-1905A>G
NM_001369404.1:c.113-1905A>G NP_001356333.1:n.113-1905A>G
NM_003476.5:c.164A>G MANE Select NP_003467.1:p.Glu55Gly
Search 100 bp 5'
Search 100 bp 3'