Canonical Allele Identifier: CA379888420
Gene: CSRP3 HGNC NCBI

Linked Data

dbSNP Id: rs1174058654
COSMIC: COSM122394

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188290C>T , CM000673.2:g.19188290C>T GRCh38
NC_000011.9:g.19209837C>T , CM000673.1:g.19209837C>T GRCh37
NC_000011.8:g.19166413C>T NCBI36
NG_011932.2:g.27284G>A , LRG_440:g.27284G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.127G>A MANE Select ENSP00000265968.3:p.Ala43Thr
ENST00000533783.2:c.127G>A ENSP00000431813.1:p.Ala43Thr
ENST00000647990.1:c.127G>A ENSP00000496798.1:p.Ala43Thr
ENST00000648719.1:c.113-3245G>A ENSP00000497633.1:n.113-3245G>A
ENST00000649235.1:c.127G>A ENSP00000497388.1:p.Ala43Thr
ENST00000649842.1:c.113-1942G>A ENSP00000497531.1:n.113-1942G>A
ENST00000265968.7:c.127G>A ENSP00000265968.3:p.Ala43Thr
ENST00000533783.1:c.127G>A ENSP00000431813.1:p.Ala43Thr
NM_003476.4:c.127G>A NP_003467.1:p.Ala43Thr
XM_024448698.1:c.113-1942G>A XP_024304466.1:n.113-1942G>A
NM_001369404.1:c.113-1942G>A NP_001356333.1:n.113-1942G>A
NM_003476.5:c.127G>A MANE Select NP_003467.1:p.Ala43Thr