Canonical Allele Identifier: CA218633129
Community Standard Title: NM_003476.5(CSRP3):c.282-147C>T
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19186495G>A , CM000673.2:g.19186495G>A GRCh38
NC_000011.9:g.19208042G>A , CM000673.1:g.19208042G>A GRCh37
NC_000011.8:g.19164618G>A NCBI36
NG_011932.2:g.29079C>T , LRG_440:g.29079C>T

Transcript Alleles

HGVS Amino-acid Change
NM_003476.5:c.282-147C>T MANE Select NP_003467.1:n.282-147C>T
ENST00000265968.9:c.282-147C>T MANE Select ENSP00000265968.3:n.282-147C>T
NM_001369404.1:c.113-147C>T NP_001356333.1:n.113-147C>T
NM_003476.4:c.282-147C>T NP_003467.1:n.282-147C>T
ENST00000265968.7:c.282-147C>T ENSP00000265968.3:n.282-147C>T
ENST00000533783.1:c.282-147C>T ENSP00000431813.1:n.282-147C>T
ENST00000533783.2:c.282-147C>T ENSP00000431813.1:n.282-147C>T
ENST00000647990.1:c.282-1450C>T ENSP00000496798.1:n.282-1450C>T
ENST00000648719.1:c.113-1450C>T ENSP00000497633.1:n.113-1450C>T
ENST00000649235.1:c.282-147C>T ENSP00000497388.1:n.282-147C>T
ENST00000649842.1:c.113-147C>T ENSP00000497531.1:n.113-147C>T
XM_024448698.1:c.113-147C>T XP_024304466.1:n.113-147C>T