Canonical Allele Identifier: CA1955949161
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19184864G= , CM000673.2:g.19184864G= GRCh38
NC_000011.9:g.19206411G= , CM000673.1:g.19206411G= GRCh37
NC_000011.8:g.19162987G= NCBI36
NG_011932.2:g.30710C= , LRG_440:g.30710C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.508+88C= MANE Select ENSP00000265968.3:n.508+88C=
ENST00000533783.2:c.508+88C= ENSP00000431813.1:n.508+88C=
ENST00000647990.1:c.375+88C= ENSP00000496798.1:n.375+88C=
ENST00000648719.1:c.*26+88C= ENSP00000497633.1:n.*26+88C=
ENST00000649235.1:c.508+88C= ENSP00000497388.1:n.508+88C=
ENST00000649842.1:c.339+88C= ENSP00000497531.1:n.339+88C=
ENST00000265968.7:c.508+88C= ENSP00000265968.3:n.508+88C=
ENST00000533783.1:c.508+88C= ENSP00000431813.1:n.508+88C=
NM_003476.4:c.508+88C= NP_003467.1:n.508+88C=
XM_024448698.1:c.339+88C= XP_024304466.1:n.339+88C=
NM_001369404.1:c.339+88C= NP_001356333.1:n.339+88C=
NM_003476.5:c.508+88C= MANE Select NP_003467.1:n.508+88C=