Canonical Allele Identifier: CA8982134

Gene: PIGN

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62102800C>T , CM000680.2:g.62102800C>T	GRCh38
NC_000018.9:g.59770033C>T , CM000680.1:g.59770033C>T	GRCh37
NC_000018.8:g.57921013C>T	NCBI36
NG_033144.1:g.89257G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_176787.5:c.1962G>A MANE Select	NP_789744.1:p.Leu654=
ENST00000640252.2:c.1962G>A MANE Select	ENSP00000492233.1:p.Leu654=
NM_012327.5:c.1962G>A	NP_036459.1:p.Leu654=
NM_012327.6:c.1962G>A	NP_036459.1:p.Leu654=
NM_176787.4:c.1962G>A	NP_789744.1:p.Leu654=
ENST00000357637.10:c.1962G>A	ENSP00000350263.4:p.Leu654=
ENST00000357637.9:c.1962G>A	ENSP00000350263.4:p.Leu654=
ENST00000400334.7:c.1962G>A	ENSP00000383188.2:p.Leu654=
ENST00000587942.1:n.824G>A
ENST00000638167.1:c.1560G>A	ENSP00000491549.1:p.Leu520=
ENST00000638183.1:c.1962G>A	ENSP00000491013.1:p.Leu654=
ENST00000638369.1:c.1779G>A	ENSP00000491811.1:p.Leu593=
ENST00000638424.1:c.1962G>A	ENSP00000491963.1:p.Leu654=
ENST00000638435.1:c.1731G>A	ENSP00000491850.1:p.Leu577=
ENST00000638858.1:n.1941G>A
ENST00000638904.1:c.1962G>A	ENSP00000491318.1:p.Leu654=
ENST00000638936.1:c.1962G>A	ENSP00000492592.1:p.Leu654=
ENST00000638977.1:c.1902G>A	ENSP00000491010.1:p.Leu634=
ENST00000639174.1:c.1962G>A	ENSP00000492783.1:p.Leu654=
ENST00000639342.1:c.1710G>A	ENSP00000491022.1:p.Leu570=
ENST00000639372.1:c.22G>A
ENST00000639600.1:c.1432G>A
ENST00000639681.1:c.*1322G>A	ENSP00000491929.1:n.*1322G>A
ENST00000639758.1:c.1902G>A	ENSP00000491475.1:p.Leu634=
ENST00000639902.1:c.1962G>A	ENSP00000490965.1:p.Leu654=
ENST00000639912.1:c.1902G>A	ENSP00000490970.1:p.Leu634=
ENST00000640050.1:c.1962G>A	ENSP00000492051.1:p.Leu654=
ENST00000640145.1:c.1962G>A	ENSP00000491525.1:p.Leu654=
ENST00000640170.1:c.*1322G>A	ENSP00000491270.1:n.*1322G>A
ENST00000640268.1:c.*107G>A	ENSP00000491111.1:n.*107G>A
ENST00000640540.1:c.1962G>A	ENSP00000491620.1:p.Leu654=
ENST00000640593.1:c.*920G>A	ENSP00000492017.1:n.*920G>A
ENST00000640682.1:c.777G>A	ENSP00000491415.1:p.Leu259=
ENST00000640876.1:c.1962G>A	ENSP00000491628.1:p.Leu654=
XM_011525889.1:c.1962G>A	XP_011524191.1:p.Leu654=
XM_011525890.1:c.1962G>A	XP_011524192.1:p.Leu654=
XM_011525891.1:c.1962G>A	XP_011524193.1:p.Leu654=
XM_011525892.1:c.1962G>A	XP_011524194.1:p.Leu654=
XM_011525893.1:c.1962G>A	XP_011524195.1:p.Leu654=
XM_011525894.1:c.1962G>A	XP_011524196.1:p.Leu654=
XM_011525895.1:c.1962G>A	XP_011524197.1:p.Leu654=
XM_011525896.1:c.1962G>A	XP_011524198.1:p.Leu654=
XM_011525897.1:c.1902G>A	XP_011524199.1:p.Leu634=
XM_011525898.1:c.1962G>A	XP_011524200.1:p.Leu654=
XM_017025685.1:c.1560G>A	XP_016881174.1:p.Leu520=
XM_017025686.1:c.1560G>A	XP_016881175.1:p.Leu520=