Canonical Allele Identifier: CA796480332

Gene: EXOC1

Linked Data

• dbSNP Id: rs1306537109
• MyVariant Identifiers: chr4:g.56751498_56751502del (hg19) ; chr4:g.55885332_55885336del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55885335_55885339del , CM000666.2:g.55885335_55885339del	GRCh38
NC_000004.11:g.56751501_56751505del , CM000666.1:g.56751501_56751505del	GRCh37
NC_000004.10:g.56446258_56446262del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381295.7:c.1330+1407_1330+1411del MANE Select	ENSP00000370695.2:n.1330+1407_1330+1411del
ENST00000346134.11:c.1330+1407_1330+1411del	ENSP00000326514.7:n.1330+1407_1330+1411del
ENST00000349598.6:c.1330+1407_1330+1411del	ENSP00000334431.6:n.1330+1407_1330+1411del
ENST00000381295.6:c.1330+1407_1330+1411del	ENSP00000370695.2:n.1330+1407_1330+1411del
ENST00000509302.5:n.161+1407_161+1411del
ENST00000511971.5:n.1202+1407_1202+1411del
NM_001024924.1:c.1330+1407_1330+1411del	NP_001020095.1:n.1330+1407_1330+1411del
NM_018261.3:c.1330+1407_1330+1411del	NP_060731.2:n.1330+1407_1330+1411del
NM_178237.2:c.1330+1407_1330+1411del	NP_839955.1:n.1330+1407_1330+1411del
XM_005265747.1:c.1384+1407_1384+1411del	XP_005265804.1:n.1384+1407_1384+1411del
XM_005265748.1:c.1384+1407_1384+1411del	XP_005265805.1:n.1384+1407_1384+1411del
XM_005265750.1:c.1330+1407_1330+1411del	XP_005265807.1:n.1330+1407_1330+1411del
XM_011534388.1:c.1405+1407_1405+1411del	XP_011532690.1:n.1405+1407_1405+1411del
XM_011534389.1:c.1405+1407_1405+1411del	XP_011532691.1:n.1405+1407_1405+1411del
XM_011534390.1:c.1405+1407_1405+1411del	XP_011532692.1:n.1405+1407_1405+1411del
XM_011534391.1:c.1351+1407_1351+1411del	XP_011532693.1:n.1351+1407_1351+1411del
XM_011534392.1:c.1351+1407_1351+1411del	XP_011532694.1:n.1351+1407_1351+1411del
XM_011534393.1:c.1405+1407_1405+1411del	XP_011532695.1:n.1405+1407_1405+1411del
XM_005265747.3:c.1384+1407_1384+1411del	XP_005265804.1:n.1384+1407_1384+1411del
XM_005265750.3:c.1330+1407_1330+1411del	XP_005265807.1:n.1330+1407_1330+1411del
XM_017008405.2:c.1384+1407_1384+1411del	XP_016863894.1:n.1384+1407_1384+1411del
XM_017008406.1:c.1384+1407_1384+1411del	XP_016863895.1:n.1384+1407_1384+1411del
XM_017008407.2:c.1384+1407_1384+1411del	XP_016863896.1:n.1384+1407_1384+1411del
XM_017008408.2:c.157+1407_157+1411del	XP_016863897.1:n.157+1407_157+1411del
XM_017008409.1:c.157+1407_157+1411del	XP_016863898.1:n.157+1407_157+1411del
XR_001741285.2:n.1689+1407_1689+1411del
XR_001741286.1:n.1490+1407_1490+1411del
NM_001024924.2:c.1330+1407_1330+1411del MANE Select	NP_001020095.1:n.1330+1407_1330+1411del
NM_018261.4:c.1330+1407_1330+1411del	NP_060731.2:n.1330+1407_1330+1411del
NM_178237.3:c.1330+1407_1330+1411del	NP_839955.1:n.1330+1407_1330+1411del