Canonical Allele Identifier: CA2249995852

Gene: PIGL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16313531_16313533delinsCTG , CM000679.2:g.16313531_16313533delinsCTG	GRCh38
NC_000017.10:g.16216845_16216847delinsCTG , CM000679.1:g.16216845_16216847delinsCTG	GRCh37
NC_000017.9:g.16157570_16157572delinsCTG	NCBI36
NG_032651.1:g.101337_101339delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225609.10:c.427-16_427-14delinsCTG MANE Select	ENSP00000225609.5:n.427-16_427-14delinsCTG
ENST00000225609.9:c.427-16_427-14delinsCTG	ENSP00000225609.5:n.427-16_427-14delinsCTG
ENST00000395844.8:c.427-16_427-14delinsCTG	ENSP00000379185.3:n.427-16_427-14delinsCTG
ENST00000477745.5:n.425-16_425-14delinsCTG
ENST00000498772.6:n.444-16_444-14delinsCTG
ENST00000580201.1:n.439-16_439-14delinsCTG
ENST00000581006.5:c.426+13553_426+13555delinsCTG	ENSP00000462432.1:n.426+13553_426+13555delinsCTG
ENST00000584797.5:c.427-16_427-14delinsCTG	ENSP00000463540.1:n.427-16_427-14delinsCTG
ENST00000585034.5:c.*21-16_*21-14delinsCTG	ENSP00000464424.1:n.*21-16_*21-14delinsCTG
NM_004278.3:c.427-16_427-14delinsCTG	NP_004269.1:n.427-16_427-14delinsCTG
XM_011524080.1:c.427-16_427-14delinsCTG	XP_011522382.1:n.427-16_427-14delinsCTG
XR_243571.2:n.445-16_445-14delinsCTG
XR_429826.2:n.445-16_445-14delinsCTG
XM_011524080.2:c.427-16_427-14delinsCTG	XP_011522382.1:n.427-16_427-14delinsCTG
XM_017025349.1:c.427-16_427-14delinsCTG	XP_016880838.1:n.427-16_427-14delinsCTG
XM_017025350.1:c.427-16_427-14delinsCTG	XP_016880839.1:n.427-16_427-14delinsCTG
XM_017025351.1:c.427-16_427-14delinsCTG	XP_016880840.1:n.427-16_427-14delinsCTG
XM_017025352.1:c.427-16_427-14delinsCTG	XP_016880841.1:n.427-16_427-14delinsCTG
XM_017025353.1:c.427-16_427-14delinsCTG	XP_016880842.1:n.427-16_427-14delinsCTG
XM_017025354.1:c.427-16_427-14delinsCTG	XP_016880843.1:n.427-16_427-14delinsCTG
XM_017025355.1:c.427-16_427-14delinsCTG	XP_016880844.1:n.427-16_427-14delinsCTG
XM_017025356.1:c.427-16_427-14delinsCTG	XP_016880845.1:n.427-16_427-14delinsCTG
NM_004278.4:c.427-16_427-14delinsCTG MANE Select	NP_004269.1:n.427-16_427-14delinsCTG