Canonical Allele Identifier: CA2612792290

Gene: CSRP3

Linked Data

• gnomAD v4: 11-19184868-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19184868G>C , CM000673.2:g.19184868G>C	GRCh38
NC_000011.9:g.19206415G>C , CM000673.1:g.19206415G>C	GRCh37
NC_000011.8:g.19162991G>C	NCBI36
NG_011932.2:g.30706C>G , LRG_440:g.30706C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.508+84C>G MANE Select	ENSP00000265968.3:n.508+84C>G
ENST00000533783.2:c.508+84C>G	ENSP00000431813.1:n.508+84C>G
ENST00000647990.1:c.375+84C>G	ENSP00000496798.1:n.375+84C>G
ENST00000648719.1:c.*26+84C>G	ENSP00000497633.1:n.*26+84C>G
ENST00000649235.1:c.508+84C>G	ENSP00000497388.1:n.508+84C>G
ENST00000649842.1:c.339+84C>G	ENSP00000497531.1:n.339+84C>G
ENST00000265968.7:c.508+84C>G	ENSP00000265968.3:n.508+84C>G
ENST00000533783.1:c.508+84C>G	ENSP00000431813.1:n.508+84C>G
NM_003476.4:c.508+84C>G	NP_003467.1:n.508+84C>G
XM_024448698.1:c.339+84C>G	XP_024304466.1:n.339+84C>G
NM_001369404.1:c.339+84C>G	NP_001356333.1:n.339+84C>G
NM_003476.5:c.508+84C>G MANE Select	NP_003467.1:n.508+84C>G