Canonical Allele Identifier: CA379887699

Gene: CSRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19184995C>G , CM000673.2:g.19184995C>G	GRCh38
NC_000011.9:g.19206542C>G , CM000673.1:g.19206542C>G	GRCh37
NC_000011.8:g.19163118C>G	NCBI36
NG_011932.2:g.30579G>C , LRG_440:g.30579G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.465G>C MANE Select	ENSP00000265968.3:p.Glu155Asp
ENST00000533783.2:c.465G>C	ENSP00000431813.1:p.Glu155Asp
ENST00000647990.1:c.332G>C	ENSP00000496798.1:p.Ser111Thr
ENST00000648719.1:c.163G>C	ENSP00000497633.1:p.Val55Leu
ENST00000649235.1:c.465G>C	ENSP00000497388.1:p.Glu155Asp
ENST00000649842.1:c.296G>C	ENSP00000497531.1:p.Ser99Thr
ENST00000265968.7:c.465G>C	ENSP00000265968.3:p.Glu155Asp
ENST00000533783.1:c.465G>C	ENSP00000431813.1:p.Glu155Asp
NM_003476.4:c.465G>C	NP_003467.1:p.Glu155Asp
XM_024448698.1:c.296G>C	XP_024304466.1:p.Ser99Thr
NM_001369404.1:c.296G>C	NP_001356333.1:p.Ser99Thr
NM_003476.5:c.465G>C MANE Select	NP_003467.1:p.Glu155Asp