Canonical Allele Identifier: CA412841898
Gene: PORCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48511352A>C , CM000685.2:g.48511352A>C GRCh38
NC_000023.10:g.48369740A>C , CM000685.1:g.48369740A>C GRCh37
NC_000023.9:g.48254684A>C NCBI36
NG_009278.1:g.7370A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367574.9:c.194A>C ENSP00000356546.6:p.Tyr65Ser
ENST00000537758.6:c.194A>C ENSP00000446401.3:p.Tyr65Ser
ENST00000682661.1:n.353A>C
ENST00000683923.1:c.194A>C ENSP00000506737.1:p.Tyr65Ser
ENST00000684722.1:n.376A>C
ENST00000326194.11:c.194A>C MANE Select ENSP00000322304.6:p.Tyr65Ser
ENST00000485288.7:c.137-14A>C ENSP00000420445.3:n.137-14A>C
ENST00000326194.10:c.194A>C ENSP00000322304.6:p.Tyr65Ser
ENST00000355092.4:c.59A>C ENSP00000347207.4:p.Tyr20Ser
ENST00000355961.8:c.194A>C ENSP00000348233.4:p.Tyr65Ser
ENST00000359882.8:c.194A>C ENSP00000352946.4:p.Tyr65Ser
ENST00000361988.7:c.194A>C ENSP00000354978.3:p.Tyr65Ser
ENST00000367574.8:c.194A>C ENSP00000356546.5:p.Tyr65Ser
ENST00000470275.2:c.137-14A>C ENSP00000418644.2:n.137-14A>C
ENST00000472520.5:c.137-540A>C ENSP00000419858.1:n.137-540A>C
ENST00000485288.6:c.329-14A>C ENSP00000420445.2:n.329-14A>C
ENST00000486272.1:n.544A>C
ENST00000489940.5:c.194A>C ENSP00000419212.1:p.Tyr65Ser
ENST00000491243.5:n.247-14A>C
ENST00000528612.5:c.137-14A>C ENSP00000431224.1:n.137-14A>C
ENST00000537758.5:c.194A>C ENSP00000446401.2:p.Tyr65Ser
NM_001282167.1:c.-6-14A>C NP_001269096.1:n.-6-14A>C
NM_022825.3:c.194A>C NP_073736.2:p.Tyr65Ser
NM_203473.2:c.194A>C NP_982299.1:p.Tyr65Ser
NM_203474.1:c.194A>C NP_982300.1:p.Tyr65Ser
NM_203475.2:c.194A>C NP_982301.1:p.Tyr65Ser
XM_005272635.1:c.533A>C XP_005272692.1:p.Tyr178Ser
XM_005272636.1:c.533A>C XP_005272693.1:p.Tyr178Ser
XM_005272637.1:c.446A>C XP_005272694.1:p.Tyr149Ser
XM_006724544.2:c.299A>C XP_006724607.1:p.Tyr100Ser
XM_006724545.2:c.259-14A>C XP_006724608.1:n.259-14A>C
XM_006724546.2:c.194A>C XP_006724609.1:p.Tyr65Ser
XM_006724547.1:c.-6-14A>C XP_006724610.1:n.-6-14A>C
XM_011543948.1:c.-6-14A>C XP_011542250.1:n.-6-14A>C
XM_024452425.1:c.533A>C XP_024308193.1:p.Tyr178Ser
NM_001282167.2:c.-6-14A>C NP_001269096.1:n.-6-14A>C
NM_022825.4:c.194A>C NP_073736.2:p.Tyr65Ser
NM_203473.3:c.194A>C NP_982299.1:p.Tyr65Ser
NM_203475.3:c.194A>C MANE Select NP_982301.1:p.Tyr65Ser