Canonical Allele Identifier: CA1955950777
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188472A= , CM000673.2:g.19188472A= GRCh38
NC_000011.9:g.19210019A= , CM000673.1:g.19210019A= GRCh37
NC_000011.8:g.19166595A= NCBI36
NG_011932.2:g.27102T= , LRG_440:g.27102T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.113-168T= MANE Select ENSP00000265968.3:n.113-168T=
ENST00000533783.2:c.113-168T= ENSP00000431813.1:n.113-168T=
ENST00000647990.1:c.113-168T= ENSP00000496798.1:n.113-168T=
ENST00000648719.1:c.113-3427T= ENSP00000497633.1:n.113-3427T=
ENST00000649235.1:c.113-168T= ENSP00000497388.1:n.113-168T=
ENST00000649842.1:c.113-2124T= ENSP00000497531.1:n.113-2124T=
ENST00000265968.7:c.113-168T= ENSP00000265968.3:n.113-168T=
ENST00000533783.1:c.113-168T= ENSP00000431813.1:n.113-168T=
NM_003476.4:c.113-168T= NP_003467.1:n.113-168T=
XM_024448698.1:c.113-2124T= XP_024304466.1:n.113-2124T=
NM_001369404.1:c.113-2124T= NP_001356333.1:n.113-2124T=
NM_003476.5:c.113-168T= MANE Select NP_003467.1:n.113-168T=