Canonical Allele Identifier: CA516010226

Gene: PORCN

Linked Data

• COSMIC: COSM3561938
• MyVariant Identifiers: chrX:g.48369807C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48511419C>T , CM000685.2:g.48511419C>T	GRCh38
NC_000023.10:g.48369807C>T , CM000685.1:g.48369807C>T	GRCh37
NC_000023.9:g.48254751C>T	NCBI36
NG_009278.1:g.7437C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367574.9:c.261C>T	ENSP00000356546.6:p.Phe87=
ENST00000537758.6:c.261C>T	ENSP00000446401.3:p.Phe87=
ENST00000682661.1:n.420C>T
ENST00000683923.1:c.261C>T	ENSP00000506737.1:p.Phe87=
ENST00000684722.1:n.443C>T
ENST00000326194.11:c.261C>T MANE Select	ENSP00000322304.6:p.Phe87=
ENST00000485288.7:c.190C>T	ENSP00000420445.3:p.Pro64Ser
ENST00000326194.10:c.261C>T	ENSP00000322304.6:p.Phe87=
ENST00000355092.4:c.126C>T	ENSP00000347207.4:p.Phe42=
ENST00000355961.8:c.261C>T	ENSP00000348233.4:p.Phe87=
ENST00000359882.8:c.261C>T	ENSP00000352946.4:p.Phe87=
ENST00000361988.7:c.261C>T	ENSP00000354978.3:p.Phe87=
ENST00000367574.8:c.261C>T	ENSP00000356546.5:p.Phe87=
ENST00000470275.2:c.190C>T	ENSP00000418644.2:p.Pro64Ser
ENST00000472520.5:c.137-473C>T	ENSP00000419858.1:n.137-473C>T
ENST00000485288.6:c.382C>T	ENSP00000420445.2:p.Pro128Ser
ENST00000489940.5:c.261C>T	ENSP00000419212.1:p.Phe87=
ENST00000491243.5:n.300C>T
ENST00000528612.5:c.190C>T	ENSP00000431224.1:p.Pro64Ser
ENST00000537758.5:c.261C>T	ENSP00000446401.2:p.Phe87=
NM_001282167.1:c.48C>T	NP_001269096.1:p.Phe16=
NM_022825.3:c.261C>T	NP_073736.2:p.Phe87=
NM_203473.2:c.261C>T	NP_982299.1:p.Phe87=
NM_203474.1:c.261C>T	NP_982300.1:p.Phe87=
NM_203475.2:c.261C>T	NP_982301.1:p.Phe87=
XM_005272635.1:c.600C>T	XP_005272692.1:p.Phe200=
XM_005272636.1:c.600C>T	XP_005272693.1:p.Phe200=
XM_005272637.1:c.513C>T	XP_005272694.1:p.Phe171=
XM_006724544.2:c.366C>T	XP_006724607.1:p.Phe122=
XM_006724545.2:c.312C>T	XP_006724608.1:p.Phe104=
XM_006724546.2:c.261C>T	XP_006724609.1:p.Phe87=
XM_006724547.1:c.48C>T	XP_006724610.1:p.Phe16=
XM_011543948.1:c.48C>T	XP_011542250.1:p.Phe16=
XM_024452425.1:c.600C>T	XP_024308193.1:p.Phe200=
NM_001282167.2:c.48C>T	NP_001269096.1:p.Phe16=
NM_022825.4:c.261C>T	NP_073736.2:p.Phe87=
NM_203473.3:c.261C>T	NP_982299.1:p.Phe87=
NM_203475.3:c.261C>T MANE Select	NP_982301.1:p.Phe87=