Canonical Allele Identifier: CA1955949151

Gene: CSRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19184834G= , CM000673.2:g.19184834G=	GRCh38
NC_000011.9:g.19206381G= , CM000673.1:g.19206381G=	GRCh37
NC_000011.8:g.19162957G=	NCBI36
NG_011932.2:g.30740C= , LRG_440:g.30740C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.508+118C= MANE Select	ENSP00000265968.3:n.508+118C=
ENST00000533783.2:c.508+118C=	ENSP00000431813.1:n.508+118C=
ENST00000647990.1:c.375+118C=	ENSP00000496798.1:n.375+118C=
ENST00000648719.1:c.*26+118C=	ENSP00000497633.1:n.*26+118C=
ENST00000649235.1:c.508+118C=	ENSP00000497388.1:n.508+118C=
ENST00000649842.1:c.339+118C=	ENSP00000497531.1:n.339+118C=
ENST00000265968.7:c.508+118C=	ENSP00000265968.3:n.508+118C=
ENST00000533783.1:c.508+118C=	ENSP00000431813.1:n.508+118C=
NM_003476.4:c.508+118C=	NP_003467.1:n.508+118C=
XM_024448698.1:c.339+118C=	XP_024304466.1:n.339+118C=
NM_001369404.1:c.339+118C=	NP_001356333.1:n.339+118C=
NM_003476.5:c.508+118C= MANE Select	NP_003467.1:n.508+118C=