Canonical Allele Identifier: CA2612792268

Gene: CSRP3

Linked Data

• gnomAD v4: 11-19184842-GCCATACCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19184845_19184852del , CM000673.2:g.19184845_19184852del	GRCh38
NC_000011.9:g.19206392_19206399del , CM000673.1:g.19206392_19206399del	GRCh37
NC_000011.8:g.19162968_19162975del	NCBI36
NG_011932.2:g.30724_30731del , LRG_440:g.30724_30731del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.508+102_508+109del MANE Select	ENSP00000265968.3:n.508+102_508+109del
ENST00000533783.2:c.508+102_508+109del	ENSP00000431813.1:n.508+102_508+109del
ENST00000647990.1:c.375+102_375+109del	ENSP00000496798.1:n.375+102_375+109del
ENST00000648719.1:c.*26+102_*26+109del	ENSP00000497633.1:n.*26+102_*26+109del
ENST00000649235.1:c.508+102_508+109del	ENSP00000497388.1:n.508+102_508+109del
ENST00000649842.1:c.339+102_339+109del	ENSP00000497531.1:n.339+102_339+109del
ENST00000265968.7:c.508+102_508+109del	ENSP00000265968.3:n.508+102_508+109del
ENST00000533783.1:c.508+102_508+109del	ENSP00000431813.1:n.508+102_508+109del
NM_003476.4:c.508+102_508+109del	NP_003467.1:n.508+102_508+109del
XM_024448698.1:c.339+102_339+109del	XP_024304466.1:n.339+102_339+109del
NM_001369404.1:c.339+102_339+109del	NP_001356333.1:n.339+102_339+109del
NM_003476.5:c.508+102_508+109del MANE Select	NP_003467.1:n.508+102_508+109del