Canonical Allele Identifier: CA1955950596
Gene: CSRP3 HGNC NCBI

Linked Data

dbSNP Id: rs1850556468

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188144_19188145insAAGTTTGAACAA , CM000673.2:g.19188144_19188145insAAGTTTGAACAA GRCh38
NC_000011.9:g.19209691_19209692insAAGTTTGAACAA , CM000673.1:g.19209691_19209692insAAGTTTGAACAA GRCh37
NC_000011.8:g.19166267_19166268insAAGTTTGAACAA NCBI36
NG_011932.2:g.27429_27430insTTGTTCAAACTT , LRG_440:g.27429_27430insTTGTTCAAACTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.272_273insTTGTTCAAACTT MANE Select ENSP00000265968.3:p.Gln91delinsHisCysSerAsnLeu
ENST00000533783.2:c.272_273insTTGTTCAAACTT ENSP00000431813.1:p.Gln91delinsHisCysSerAsnLeu
ENST00000647990.1:c.272_273insTTGTTCAAACTT ENSP00000496798.1:p.Gln91delinsHisCysSerAsnLeu
ENST00000648719.1:c.113-3100_113-3099insTTGTTCAAACTT ENSP00000497633.1:n.113-3100_113-3099insTTGTTCAAACTT
ENST00000649235.1:c.272_273insTTGTTCAAACTT ENSP00000497388.1:p.Gln91delinsHisCysSerAsnLeu
ENST00000649842.1:c.113-1797_113-1796insTTGTTCAAACTT ENSP00000497531.1:n.113-1797_113-1796insTTGTTCAAACTT
ENST00000265968.7:c.272_273insTTGTTCAAACTT ENSP00000265968.3:p.Gln91delinsHisCysSerAsnLeu
ENST00000533783.1:c.272_273insTTGTTCAAACTT ENSP00000431813.1:p.Gln91delinsHisCysSerAsnLeu
NM_003476.4:c.272_273insTTGTTCAAACTT NP_003467.1:p.Gln91delinsHisCysSerAsnLeu
XM_024448698.1:c.113-1797_113-1796insTTGTTCAAACTT XP_024304466.1:n.113-1797_113-1796insTTGTTCAAACTT
NM_001369404.1:c.113-1797_113-1796insTTGTTCAAACTT NP_001356333.1:n.113-1797_113-1796insTTGTTCAAACTT
NM_003476.5:c.272_273insTTGTTCAAACTT MANE Select NP_003467.1:p.Gln91delinsHisCysSerAsnLeu