Canonical Allele Identifier: CA516010047
Gene: PORCN HGNC NCBI

Linked Data

COSMIC: COSM392276
MyVariant Identifiers: chrX:g.48369767del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48511381del , CM000685.2:g.48511381del GRCh38
NC_000023.10:g.48369769del , CM000685.1:g.48369769del GRCh37
NC_000023.9:g.48254713del NCBI36
NG_009278.1:g.7399del

Transcript Alleles

HGVS Amino-acid change
ENST00000367574.9:c.223del ENSP00000356546.6:p.Val75SerfsTer?
ENST00000537758.6:c.223del ENSP00000446401.3:p.Val75SerfsTer?
ENST00000682661.1:n.382del
ENST00000683923.1:c.223del ENSP00000506737.1:p.Val75SerfsTer?
ENST00000684722.1:n.405del
ENST00000326194.11:c.223del MANE Select ENSP00000322304.6:p.Val75SerfsTer?
ENST00000485288.7:c.152del ENSP00000420445.3:p.Gly51ValfsTer?
ENST00000326194.10:c.223del ENSP00000322304.6:p.Val75SerfsTer?
ENST00000355092.4:c.88del ENSP00000347207.4:p.Val30SerfsTer?
ENST00000355961.8:c.223del ENSP00000348233.4:p.Val75SerfsTer?
ENST00000359882.8:c.223del ENSP00000352946.4:p.Val75SerfsTer?
ENST00000361988.7:c.223del ENSP00000354978.3:p.Val75SerfsTer?
ENST00000367574.8:c.223del ENSP00000356546.5:p.Val75SerfsTer?
ENST00000470275.2:c.152del ENSP00000418644.2:p.Gly51ValfsTer?
ENST00000472520.5:c.137-511del ENSP00000419858.1:n.137-511del
ENST00000485288.6:c.344del ENSP00000420445.2:p.Gly115ValfsTer?
ENST00000489940.5:c.223del ENSP00000419212.1:p.Val75SerfsTer?
ENST00000491243.5:n.262del
ENST00000528612.5:c.152del ENSP00000431224.1:p.Gly51ValfsTer?
ENST00000537758.5:c.223del ENSP00000446401.2:p.Val75SerfsTer?
NM_001282167.1:c.10del NP_001269096.1:p.Val4SerfsTer?
NM_022825.3:c.223del NP_073736.2:p.Val75SerfsTer?
NM_203473.2:c.223del NP_982299.1:p.Val75SerfsTer?
NM_203474.1:c.223del NP_982300.1:p.Val75SerfsTer?
NM_203475.2:c.223del NP_982301.1:p.Val75SerfsTer?
XM_005272635.1:c.562del XP_005272692.1:p.Val188SerfsTer?
XM_005272636.1:c.562del XP_005272693.1:p.Val188SerfsTer?
XM_005272637.1:c.475del XP_005272694.1:p.Val159SerfsTer?
XM_006724544.2:c.328del XP_006724607.1:p.Val110SerfsTer?
XM_006724545.2:c.274del XP_006724608.1:p.Val92SerfsTer?
XM_006724546.2:c.223del XP_006724609.1:p.Val75SerfsTer?
XM_006724547.1:c.10del XP_006724610.1:p.Val4SerfsTer?
XM_011543948.1:c.10del XP_011542250.1:p.Val4SerfsTer?
XM_024452425.1:c.562del XP_024308193.1:p.Val188SerfsTer?
NM_001282167.2:c.10del NP_001269096.1:p.Val4SerfsTer?
NM_022825.4:c.223del NP_073736.2:p.Val75SerfsTer?
NM_203473.3:c.223del NP_982299.1:p.Val75SerfsTer?
NM_203475.3:c.223del MANE Select NP_982301.1:p.Val75SerfsTer?