Canonical Allele Identifier: CA1955950664
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188258C= , CM000673.2:g.19188258C= GRCh38
NC_000011.9:g.19209805C= , CM000673.1:g.19209805C= GRCh37
NC_000011.8:g.19166381C= NCBI36
NG_011932.2:g.27316G= , LRG_440:g.27316G=

Transcript Alleles

HGVS Amino-acid change
ENST00000265968.9:c.159G= MANE Select ENSP00000265968.3:p.Glu53=
ENST00000533783.2:c.159G= ENSP00000431813.1:p.Glu53=
ENST00000647990.1:c.159G= ENSP00000496798.1:p.Glu53=
ENST00000648719.1:c.113-3213G= ENSP00000497633.1:n.113-3213G=
ENST00000649235.1:c.159G= ENSP00000497388.1:p.Glu53=
ENST00000649842.1:c.113-1910G= ENSP00000497531.1:n.113-1910G=
ENST00000265968.7:c.159G= ENSP00000265968.3:p.Glu53=
ENST00000533783.1:c.159G= ENSP00000431813.1:p.Glu53=
NM_003476.4:c.159G= NP_003467.1:p.Glu53=
XM_024448698.1:c.113-1910G= XP_024304466.1:n.113-1910G=
NM_001369404.1:c.113-1910G= NP_001356333.1:n.113-1910G=
NM_003476.5:c.159G= MANE Select NP_003467.1:p.Glu53=