Canonical Allele Identifier: CA379888438
Gene: CSRP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188298C>A , CM000673.2:g.19188298C>A GRCh38
NC_000011.9:g.19209845C>A , CM000673.1:g.19209845C>A GRCh37
NC_000011.8:g.19166421C>A NCBI36
NG_011932.2:g.27276G>T , LRG_440:g.27276G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.119G>T MANE Select ENSP00000265968.3:p.Cys40Phe
ENST00000533783.2:c.119G>T ENSP00000431813.1:p.Cys40Phe
ENST00000647990.1:c.119G>T ENSP00000496798.1:p.Cys40Phe
ENST00000648719.1:c.113-3253G>T ENSP00000497633.1:n.113-3253G>T
ENST00000649235.1:c.119G>T ENSP00000497388.1:p.Cys40Phe
ENST00000649842.1:c.113-1950G>T ENSP00000497531.1:n.113-1950G>T
ENST00000265968.7:c.119G>T ENSP00000265968.3:p.Cys40Phe
ENST00000533783.1:c.119G>T ENSP00000431813.1:p.Cys40Phe
NM_003476.4:c.119G>T NP_003467.1:p.Cys40Phe
XM_024448698.1:c.113-1950G>T XP_024304466.1:n.113-1950G>T
NM_001369404.1:c.113-1950G>T NP_001356333.1:n.113-1950G>T
NM_003476.5:c.119G>T MANE Select NP_003467.1:p.Cys40Phe