Canonical Allele Identifier: CA402606171

Gene: PIGN

Linked Data

• gnomAD v4: 18-62114609-A-C
• MyVariant Identifiers: chr18:g.59781842A>C (hg19) ; chr18:g.62114609A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62114609A>C , CM000680.2:g.62114609A>C	GRCh38
NC_000018.9:g.59781842A>C , CM000680.1:g.59781842A>C	GRCh37
NC_000018.8:g.57932822A>C	NCBI36
NG_033144.1:g.77448T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000357637.10:c.1203T>G	ENSP00000350263.4:p.Ile401Met
ENST00000588571.6:c.1203T>G	ENSP00000466035.2:p.Ile401Met
ENST00000589339.6:c.1203T>G	ENSP00000465506.2:p.Ile401Met
ENST00000638167.1:c.1173-7524T>G	ENSP00000491549.1:n.1173-7524T>G
ENST00000638183.1:c.1203T>G	ENSP00000491013.1:p.Ile401Met
ENST00000638329.1:c.1203T>G	ENSP00000492804.1:p.Ile401Met
ENST00000638369.1:c.1203T>G	ENSP00000491811.1:p.Ile401Met
ENST00000638424.1:c.1203T>G	ENSP00000491963.1:p.Ile401Met
ENST00000638435.1:c.972T>G	ENSP00000491850.1:p.Ile324Met
ENST00000638858.1:n.1182T>G
ENST00000638904.1:c.1203T>G	ENSP00000491318.1:p.Ile401Met
ENST00000638936.1:c.1203T>G	ENSP00000492592.1:p.Ile401Met
ENST00000638977.1:c.1143T>G	ENSP00000491010.1:p.Ile381Met
ENST00000639174.1:c.1203T>G	ENSP00000492783.1:p.Ile401Met
ENST00000639214.1:n.1444T>G
ENST00000639342.1:c.951T>G	ENSP00000491022.1:p.Ile317Met
ENST00000639600.1:c.673T>G
ENST00000639681.1:c.*563T>G	ENSP00000491929.1:n.*563T>G
ENST00000639758.1:c.1143T>G	ENSP00000491475.1:p.Ile381Met
ENST00000639902.1:c.1203T>G	ENSP00000490965.1:p.Ile401Met
ENST00000639912.1:c.1143T>G	ENSP00000490970.1:p.Ile381Met
ENST00000640050.1:c.1203T>G	ENSP00000492051.1:p.Ile401Met
ENST00000640145.1:c.1203T>G	ENSP00000491525.1:p.Ile401Met
ENST00000640170.1:c.*563T>G	ENSP00000491270.1:n.*563T>G
ENST00000640252.2:c.1203T>G MANE Select	ENSP00000492233.1:p.Ile401Met
ENST00000640268.1:c.1203T>G	ENSP00000491111.1:p.Ile401Met
ENST00000640540.1:c.1203T>G	ENSP00000491620.1:p.Ile401Met
ENST00000640593.1:c.*533-7524T>G	ENSP00000492017.1:n.*533-7524T>G
ENST00000640682.1:c.18T>G	ENSP00000491415.1:p.Ile6Met
ENST00000640876.1:c.1203T>G	ENSP00000491628.1:p.Ile401Met
ENST00000357637.9:c.1203T>G	ENSP00000350263.4:p.Ile401Met
ENST00000400334.7:c.1203T>G	ENSP00000383188.2:p.Ile401Met
ENST00000586566.1:c.45-7524T>G	ENSP00000467410.1:n.45-7524T>G
NM_012327.5:c.1203T>G	NP_036459.1:p.Ile401Met
NM_176787.4:c.1203T>G	NP_789744.1:p.Ile401Met
XM_011525889.1:c.1203T>G	XP_011524191.1:p.Ile401Met
XM_011525890.1:c.1203T>G	XP_011524192.1:p.Ile401Met
XM_011525891.1:c.1203T>G	XP_011524193.1:p.Ile401Met
XM_011525892.1:c.1203T>G	XP_011524194.1:p.Ile401Met
XM_011525893.1:c.1203T>G	XP_011524195.1:p.Ile401Met
XM_011525894.1:c.1203T>G	XP_011524196.1:p.Ile401Met
XM_011525895.1:c.1203T>G	XP_011524197.1:p.Ile401Met
XM_011525896.1:c.1203T>G	XP_011524198.1:p.Ile401Met
XM_011525897.1:c.1143T>G	XP_011524199.1:p.Ile381Met
XM_011525898.1:c.1203T>G	XP_011524200.1:p.Ile401Met
XM_017025685.1:c.1173-7524T>G	XP_016881174.1:n.1173-7524T>G
XM_017025686.1:c.1173-7524T>G	XP_016881175.1:n.1173-7524T>G
NM_176787.5:c.1203T>G MANE Select	NP_789744.1:p.Ile401Met
NM_012327.6:c.1203T>G	NP_036459.1:p.Ile401Met