Canonical Allele Identifier: CA96945368
Gene: EXOC1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs13117307

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55885574C>T , CM000666.2:g.55885574C>T GRCh38
NC_000004.11:g.56751740C>T , CM000666.1:g.56751740C>T GRCh37
NC_000004.10:g.56446497C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001024924.1:c.1330+1646C>T VV NP_001020095.1:p.=
NM_018261.3:c.1330+1646C>T VV NP_060731.2:p.=
NM_178237.2:c.1330+1646C>T VV NP_839955.1:p.=
XM_005265747.1:c.1384+1646C>T XP_005265804.1:p.=
XM_005265748.1:c.1384+1646C>T XP_005265805.1:p.=
XM_005265750.1:c.1330+1646C>T XP_005265807.1:p.=
XM_011534388.1:c.1405+1646C>T XP_011532690.1:p.=
XM_011534389.1:c.1405+1646C>T XP_011532691.1:p.=
XM_011534390.1:c.1405+1646C>T XP_011532692.1:p.=
XM_011534391.1:c.1351+1646C>T XP_011532693.1:p.=
XM_011534392.1:c.1351+1646C>T XP_011532694.1:p.=
XM_011534393.1:c.1405+1646C>T XP_011532695.1:p.=
XM_005265747.3:c.1384+1646C>T XP_005265804.1:p.=
XM_005265750.3:c.1330+1646C>T XP_005265807.1:p.=
XM_017008405.2:c.1384+1646C>T XP_016863894.1:p.=
XM_017008406.1:c.1384+1646C>T XP_016863895.1:p.=
XM_017008407.2:c.1384+1646C>T XP_016863896.1:p.=
XM_017008408.2:c.157+1646C>T XP_016863897.1:p.=
XM_017008409.1:c.157+1646C>T XP_016863898.1:p.=
XR_001741285.2:n.1689+1646C>T
XR_001741286.1:n.1490+1646C>T
NM_001024924.2:c.1330+1646C>T VV MANE Preferred NP_001020095.1:p.=
ENST00000346134.11:c.1330+1646C>T ENSP00000326514.7:p.=
ENST00000349598.6:c.1330+1646C>T ENSP00000334431.6:p.=
ENST00000381295.6:c.1330+1646C>T ENSP00000370695.2:p.=
ENST00000509302.5:n.161+1646C>T
ENST00000511971.5:n.1202+1646C>T