Canonical Allele Identifier: CA183402
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19182739A>G , CM000673.2:g.19182739A>G GRCh38
NC_000011.9:g.19204286A>G , CM000673.1:g.19204286A>G GRCh37
NC_000011.8:g.19160862A>G NCBI36
NG_011932.2:g.32835T>C , LRG_440:g.32835T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.516T>C MANE Select ENSP00000265968.3:p.Tyr172=
ENST00000533783.2:c.516T>C ENSP00000431813.1:p.Tyr172=
ENST00000647990.1:c.383T>C ENSP00000496798.1:p.Met128Thr
ENST00000648719.1:c.*34T>C ENSP00000497633.1:n.*34T>C
ENST00000649235.1:c.516T>C ENSP00000497388.1:p.Tyr172=
ENST00000649842.1:c.347T>C ENSP00000497531.1:p.Met116Thr
ENST00000265968.7:c.516T>C ENSP00000265968.3:p.Tyr172=
ENST00000533783.1:c.516T>C ENSP00000431813.1:p.Tyr172=
NM_003476.4:c.516T>C NP_003467.1:p.Tyr172=
XM_024448698.1:c.347T>C XP_024304466.1:p.Met116Thr
NM_001369404.1:c.347T>C NP_001356333.1:p.Met116Thr
NM_003476.5:c.516T>C MANE Select NP_003467.1:p.Tyr172=