Canonical Allele Identifier: CA2612793015

Gene: CSRP3

Linked Data

• gnomAD v4: 11-19188438-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188440del , CM000673.2:g.19188440del	GRCh38
NC_000011.9:g.19209987del , CM000673.1:g.19209987del	GRCh37
NC_000011.8:g.19166563del	NCBI36
NG_011932.2:g.27135del , LRG_440:g.27135del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.113-135del MANE Select	ENSP00000265968.3:n.113-135del
ENST00000533783.2:c.113-135del	ENSP00000431813.1:n.113-135del
ENST00000647990.1:c.113-135del	ENSP00000496798.1:n.113-135del
ENST00000648719.1:c.113-3394del	ENSP00000497633.1:n.113-3394del
ENST00000649235.1:c.113-135del	ENSP00000497388.1:n.113-135del
ENST00000649842.1:c.113-2091del	ENSP00000497531.1:n.113-2091del
ENST00000265968.7:c.113-135del	ENSP00000265968.3:n.113-135del
ENST00000533783.1:c.113-135del	ENSP00000431813.1:n.113-135del
NM_003476.4:c.113-135del	NP_003467.1:n.113-135del
XM_024448698.1:c.113-2091del	XP_024304466.1:n.113-2091del
NM_001369404.1:c.113-2091del	NP_001356333.1:n.113-2091del
NM_003476.5:c.113-135del MANE Select	NP_003467.1:n.113-135del