Canonical Allele Identifier: CA412841777

Gene: PORCN

Linked Data

• MyVariant Identifiers: chrX:g.48369713C>G (hg19) ; chrX:g.48511325C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48511325C>G , CM000685.2:g.48511325C>G	GRCh38
NC_000023.10:g.48369713C>G , CM000685.1:g.48369713C>G	GRCh37
NC_000023.9:g.48254657C>G	NCBI36
NG_009278.1:g.7343C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367574.9:c.167C>G	ENSP00000356546.6:p.Thr56Ser
ENST00000537758.6:c.167C>G	ENSP00000446401.3:p.Thr56Ser
ENST00000682661.1:n.326C>G
ENST00000683923.1:c.167C>G	ENSP00000506737.1:p.Thr56Ser
ENST00000684722.1:n.349C>G
ENST00000326194.11:c.167C>G MANE Select	ENSP00000322304.6:p.Thr56Ser
ENST00000485288.7:c.137-41C>G	ENSP00000420445.3:n.137-41C>G
ENST00000326194.10:c.167C>G	ENSP00000322304.6:p.Thr56Ser
ENST00000355092.4:c.32C>G	ENSP00000347207.4:p.Thr11Ser
ENST00000355961.8:c.167C>G	ENSP00000348233.4:p.Thr56Ser
ENST00000359882.8:c.167C>G	ENSP00000352946.4:p.Thr56Ser
ENST00000361988.7:c.167C>G	ENSP00000354978.3:p.Thr56Ser
ENST00000367574.8:c.167C>G	ENSP00000356546.5:p.Thr56Ser
ENST00000470275.2:c.137-41C>G	ENSP00000418644.2:n.137-41C>G
ENST00000472520.5:c.137-567C>G	ENSP00000419858.1:n.137-567C>G
ENST00000485288.6:c.329-41C>G	ENSP00000420445.2:n.329-41C>G
ENST00000486272.1:n.517C>G
ENST00000489940.5:c.167C>G	ENSP00000419212.1:p.Thr56Ser
ENST00000491243.5:n.247-41C>G
ENST00000528612.5:c.137-41C>G	ENSP00000431224.1:n.137-41C>G
ENST00000537758.5:c.167C>G	ENSP00000446401.2:p.Thr56Ser
NM_001282167.1:c.-6-41C>G	NP_001269096.1:n.-6-41C>G
NM_022825.3:c.167C>G	NP_073736.2:p.Thr56Ser
NM_203473.2:c.167C>G	NP_982299.1:p.Thr56Ser
NM_203474.1:c.167C>G	NP_982300.1:p.Thr56Ser
NM_203475.2:c.167C>G	NP_982301.1:p.Thr56Ser
XM_005272635.1:c.506C>G	XP_005272692.1:p.Thr169Ser
XM_005272636.1:c.506C>G	XP_005272693.1:p.Thr169Ser
XM_005272637.1:c.419C>G	XP_005272694.1:p.Thr140Ser
XM_006724544.2:c.272C>G	XP_006724607.1:p.Thr91Ser
XM_006724545.2:c.259-41C>G	XP_006724608.1:n.259-41C>G
XM_006724546.2:c.167C>G	XP_006724609.1:p.Thr56Ser
XM_006724547.1:c.-6-41C>G	XP_006724610.1:n.-6-41C>G
XM_011543948.1:c.-6-41C>G	XP_011542250.1:n.-6-41C>G
XM_024452425.1:c.506C>G	XP_024308193.1:p.Thr169Ser
NM_001282167.2:c.-6-41C>G	NP_001269096.1:n.-6-41C>G
NM_022825.4:c.167C>G	NP_073736.2:p.Thr56Ser
NM_203473.3:c.167C>G	NP_982299.1:p.Thr56Ser
NM_203475.3:c.167C>G MANE Select	NP_982301.1:p.Thr56Ser