Canonical Allele Identifier: CA1955950854
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188618G= , CM000673.2:g.19188618G= GRCh38
NC_000011.9:g.19210165G= , CM000673.1:g.19210165G= GRCh37
NC_000011.8:g.19166741G= NCBI36
NG_011932.2:g.26956C= , LRG_440:g.26956C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.113-314C= MANE Select ENSP00000265968.3:n.113-314C=
ENST00000533783.2:c.113-314C= ENSP00000431813.1:n.113-314C=
ENST00000647990.1:c.113-314C= ENSP00000496798.1:n.113-314C=
ENST00000648719.1:c.113-3573C= ENSP00000497633.1:n.113-3573C=
ENST00000649235.1:c.113-314C= ENSP00000497388.1:n.113-314C=
ENST00000649842.1:c.113-2270C= ENSP00000497531.1:n.113-2270C=
ENST00000265968.7:c.113-314C= ENSP00000265968.3:n.113-314C=
ENST00000533783.1:c.113-314C= ENSP00000431813.1:n.113-314C=
NM_003476.4:c.113-314C= NP_003467.1:n.113-314C=
XM_024448698.1:c.113-2270C= XP_024304466.1:n.113-2270C=
NM_001369404.1:c.113-2270C= NP_001356333.1:n.113-2270C=
NM_003476.5:c.113-314C= MANE Select NP_003467.1:n.113-314C=