Canonical Allele Identifier: CA8982014

Gene: PIGN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62088843C>G , CM000680.2:g.62088843C>G	GRCh38
NC_000018.9:g.59756076C>G , CM000680.1:g.59756076C>G	GRCh37
NC_000018.8:g.57907056C>G	NCBI36
NG_033144.1:g.103214G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357637.10:c.2284-1G>C	ENSP00000350263.4:n.2284-1G>C
ENST00000638167.1:c.1882-1G>C	ENSP00000491549.1:n.1882-1G>C
ENST00000638183.1:c.2284-1G>C	ENSP00000491013.1:n.2284-1G>C
ENST00000638369.1:c.2101-1G>C	ENSP00000491811.1:n.2101-1G>C
ENST00000638424.1:c.2284-1G>C	ENSP00000491963.1:n.2284-1G>C
ENST00000638435.1:c.2053-1G>C	ENSP00000491850.1:n.2053-1G>C
ENST00000638858.1:n.2263-1G>C
ENST00000638904.1:c.2181-1G>C	ENSP00000491318.1:n.2181-1G>C
ENST00000638936.1:c.2284-1G>C	ENSP00000492592.1:n.2284-1G>C
ENST00000638977.1:c.2224-1G>C	ENSP00000491010.1:n.2224-1G>C
ENST00000639174.1:c.2284-1G>C	ENSP00000492783.1:n.2284-1G>C
ENST00000639342.1:c.2032-1G>C	ENSP00000491022.1:n.2032-1G>C
ENST00000639372.1:c.344-1G>C
ENST00000639600.1:c.1754-1G>C
ENST00000639681.1:c.*1541-1G>C	ENSP00000491929.1:n.*1541-1G>C
ENST00000639758.1:c.2224-1G>C	ENSP00000491475.1:n.2224-1G>C
ENST00000639902.1:c.2284-1G>C	ENSP00000490965.1:n.2284-1G>C
ENST00000639912.1:c.2224-1G>C	ENSP00000490970.1:n.2224-1G>C
ENST00000640050.1:c.2284-1G>C	ENSP00000492051.1:n.2284-1G>C
ENST00000640145.1:c.2284-1G>C	ENSP00000491525.1:n.2284-1G>C
ENST00000640170.1:c.*1644-1G>C	ENSP00000491270.1:n.*1644-1G>C
ENST00000640252.2:c.2284-1G>C MANE Select	ENSP00000492233.1:n.2284-1G>C
ENST00000640268.1:c.*429-1G>C	ENSP00000491111.1:n.*429-1G>C
ENST00000640540.1:c.2284-1G>C	ENSP00000491620.1:n.2284-1G>C
ENST00000640593.1:c.*1242-1G>C	ENSP00000492017.1:n.*1242-1G>C
ENST00000640682.1:c.1099-1G>C	ENSP00000491415.1:n.1099-1G>C
ENST00000640876.1:c.2284-1G>C	ENSP00000491628.1:n.2284-1G>C
ENST00000357637.9:c.2284-1G>C	ENSP00000350263.4:n.2284-1G>C
ENST00000400334.7:c.2284-1G>C	ENSP00000383188.2:n.2284-1G>C
ENST00000587942.1:n.1146-1G>C
NM_012327.5:c.2284-1G>C	NP_036459.1:n.2284-1G>C
NM_176787.4:c.2284-1G>C	NP_789744.1:n.2284-1G>C
XM_011525889.1:c.2284-1G>C	XP_011524191.1:n.2284-1G>C
XM_011525890.1:c.2284-1G>C	XP_011524192.1:n.2284-1G>C
XM_011525891.1:c.2284-1G>C	XP_011524193.1:n.2284-1G>C
XM_011525892.1:c.2284-1G>C	XP_011524194.1:n.2284-1G>C
XM_011525893.1:c.2284-1G>C	XP_011524195.1:n.2284-1G>C
XM_011525894.1:c.2284-1G>C	XP_011524196.1:n.2284-1G>C
XM_011525895.1:c.2284-1G>C	XP_011524197.1:n.2284-1G>C
XM_011525896.1:c.2284-1G>C	XP_011524198.1:n.2284-1G>C
XM_011525897.1:c.2224-1G>C	XP_011524199.1:n.2224-1G>C
XM_011525898.1:c.2284-1G>C	XP_011524200.1:n.2284-1G>C
XM_017025685.1:c.1882-1G>C	XP_016881174.1:n.1882-1G>C
XM_017025686.1:c.1882-1G>C	XP_016881175.1:n.1882-1G>C
NM_176787.5:c.2284-1G>C MANE Select	NP_789744.1:n.2284-1G>C
NM_012327.6:c.2284-1G>C	NP_036459.1:n.2284-1G>C