Canonical Allele Identifier: CA2428293322
Gene: PORCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48511442G= , CM000685.2:g.48511442G= GRCh38
NC_000023.10:g.48369830G= , CM000685.1:g.48369830G= GRCh37
NC_000023.9:g.48254774G= NCBI36
NG_009278.1:g.7460G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367574.9:c.284G= ENSP00000356546.6:p.Arg95=
ENST00000537758.6:c.284G= ENSP00000446401.3:p.Arg95=
ENST00000682661.1:n.443G=
ENST00000683923.1:c.284G= ENSP00000506737.1:p.Arg95=
ENST00000684722.1:n.466G=
ENST00000326194.11:c.284G= MANE Select ENSP00000322304.6:p.Arg95=
ENST00000485288.7:c.213G= ENSP00000420445.3:p.Ser71=
ENST00000326194.10:c.284G= ENSP00000322304.6:p.Arg95=
ENST00000355092.4:c.149G= ENSP00000347207.4:p.Arg50=
ENST00000355961.8:c.284G= ENSP00000348233.4:p.Arg95=
ENST00000359882.8:c.284G= ENSP00000352946.4:p.Arg95=
ENST00000361988.7:c.284G= ENSP00000354978.3:p.Arg95=
ENST00000367574.8:c.284G= ENSP00000356546.5:p.Arg95=
ENST00000470275.2:c.213G= ENSP00000418644.2:p.Ser71=
ENST00000472520.5:c.137-450G= ENSP00000419858.1:n.137-450G=
ENST00000485288.6:c.405G= ENSP00000420445.2:p.Ser135=
ENST00000489940.5:c.284G= ENSP00000419212.1:p.Arg95=
ENST00000491243.5:n.323G=
ENST00000528612.5:c.213G= ENSP00000431224.1:p.Ser71=
ENST00000537758.5:c.284G= ENSP00000446401.2:p.Arg95=
NM_001282167.1:c.71G= NP_001269096.1:p.Arg24=
NM_022825.3:c.284G= NP_073736.2:p.Arg95=
NM_203473.2:c.284G= NP_982299.1:p.Arg95=
NM_203474.1:c.284G= NP_982300.1:p.Arg95=
NM_203475.2:c.284G= NP_982301.1:p.Arg95=
XM_005272635.1:c.623G= XP_005272692.1:p.Arg208=
XM_005272636.1:c.623G= XP_005272693.1:p.Arg208=
XM_005272637.1:c.536G= XP_005272694.1:p.Arg179=
XM_006724544.2:c.389G= XP_006724607.1:p.Arg130=
XM_006724545.2:c.335G= XP_006724608.1:p.Arg112=
XM_006724546.2:c.284G= XP_006724609.1:p.Arg95=
XM_006724547.1:c.71G= XP_006724610.1:p.Arg24=
XM_011543948.1:c.71G= XP_011542250.1:p.Arg24=
XM_024452425.1:c.623G= XP_024308193.1:p.Arg208=
NM_001282167.2:c.71G= NP_001269096.1:p.Arg24=
NM_022825.4:c.284G= NP_073736.2:p.Arg95=
NM_203473.3:c.284G= NP_982299.1:p.Arg95=
NM_203475.3:c.284G= MANE Select NP_982301.1:p.Arg95=