Canonical Allele Identifier: CA641498294

Gene: PORCN

Linked Data

• dbSNP Id: rs1556973915
• gnomAD v2: X-48370031-A-G
• gnomAD v3: X-48511643-A-G
• gnomAD v4: X-48511643-A-G
• MyVariant Identifiers: chrX:g.48370031A>G (hg19) ; chrX:g.48511643A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48511643A>G , CM000685.2:g.48511643A>G	GRCh38
NC_000023.10:g.48370031A>G , CM000685.1:g.48370031A>G	GRCh37
NC_000023.9:g.48254975A>G	NCBI36
NG_009278.1:g.7661A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367574.9:c.329+156A>G	ENSP00000356546.6:n.329+156A>G
ENST00000537758.6:c.329+156A>G	ENSP00000446401.3:n.329+156A>G
ENST00000682661.1:n.488+156A>G
ENST00000683923.1:c.329+156A>G	ENSP00000506737.1:n.329+156A>G
ENST00000684722.1:n.511+156A>G
ENST00000326194.11:c.329+156A>G MANE Select	ENSP00000322304.6:n.329+156A>G
ENST00000485288.7:c.258+156A>G	ENSP00000420445.3:n.258+156A>G
ENST00000326194.10:c.329+156A>G	ENSP00000322304.6:n.329+156A>G
ENST00000355092.4:c.194+156A>G	ENSP00000347207.4:n.194+156A>G
ENST00000355961.8:c.329+156A>G	ENSP00000348233.4:n.329+156A>G
ENST00000359882.8:c.329+156A>G	ENSP00000352946.4:n.329+156A>G
ENST00000361988.7:c.329+156A>G	ENSP00000354978.3:n.329+156A>G
ENST00000367574.8:c.329+156A>G	ENSP00000356546.5:n.329+156A>G
ENST00000470275.2:c.258+156A>G	ENSP00000418644.2:n.258+156A>G
ENST00000472520.5:c.137-249A>G	ENSP00000419858.1:n.137-249A>G
ENST00000485288.6:c.450+156A>G	ENSP00000420445.2:n.450+156A>G
ENST00000491243.5:n.368+156A>G
ENST00000528612.5:c.258+156A>G	ENSP00000431224.1:n.258+156A>G
ENST00000537758.5:c.329+156A>G	ENSP00000446401.2:n.329+156A>G
NM_001282167.1:c.116+156A>G	NP_001269096.1:n.116+156A>G
NM_022825.3:c.329+156A>G	NP_073736.2:n.329+156A>G
NM_203473.2:c.329+156A>G	NP_982299.1:n.329+156A>G
NM_203474.1:c.329+156A>G	NP_982300.1:n.329+156A>G
NM_203475.2:c.329+156A>G	NP_982301.1:n.329+156A>G
XM_005272635.1:c.668+156A>G	XP_005272692.1:n.668+156A>G
XM_005272636.1:c.668+156A>G	XP_005272693.1:n.668+156A>G
XM_005272637.1:c.581+156A>G	XP_005272694.1:n.581+156A>G
XM_006724544.2:c.434+156A>G	XP_006724607.1:n.434+156A>G
XM_006724545.2:c.380+156A>G	XP_006724608.1:n.380+156A>G
XM_006724546.2:c.329+156A>G	XP_006724609.1:n.329+156A>G
XM_006724547.1:c.116+156A>G	XP_006724610.1:n.116+156A>G
XM_011543948.1:c.116+156A>G	XP_011542250.1:n.116+156A>G
XM_024452425.1:c.668+156A>G	XP_024308193.1:n.668+156A>G
NM_001282167.2:c.116+156A>G	NP_001269096.1:n.116+156A>G
NM_022825.4:c.329+156A>G	NP_073736.2:n.329+156A>G
NM_203473.3:c.329+156A>G	NP_982299.1:n.329+156A>G
NM_203475.3:c.329+156A>G MANE Select	NP_982301.1:n.329+156A>G