Canonical Allele Identifier: CA1677206036

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741432_160741433delinsAT , CM000668.2:g.160741432_160741433delinsAT	GRCh38
NC_000006.11:g.161162464_161162465delinsAT , CM000668.1:g.161162464_161162465delinsAT	GRCh37
NC_000006.10:g.161082454_161082455delinsAT	NCBI36
NG_016200.1:g.44240_44241delinsAT , LRG_571:g.44240_44241delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.1078+15_1078+16delinsAT	ENSP00000516619.1:n.1078+15_1078+16delins...
ENST00000418964.2:c.2176+15_2176+16delinsAT	ENSP00000389424.2:n.2176+15_2176+16delins...
ENST00000706906.1:c.*2145+15_*2145+16delinsAT	ENSP00000516618.1:n.*2145+15_*2145+16deli...
ENST00000308192.14:c.2125+15_2125+16delinsAT MANE Select	ENSP00000308938.9:n.2125+15_2125+16delins...
ENST00000308192.13:c.2125+15_2125+16delinsAT	ENSP00000308938.9:n.2125+15_2125+16delins...
ENST00000461414.2:n.99+64_99+65delinsAT
ENST00000467466.1:n.426+15_426+16delinsAT
NM_000301.3:c.2125+15_2125+16delinsAT , LRG_571t1:c.2125+15_2125+16delinsAT	NP_000292.1:n.2125+15_2125+16delinsAT
NM_000301.4:c.2125+15_2125+16delinsAT	NP_000292.1:n.2125+15_2125+16delinsAT
NM_000301.5:c.2125+15_2125+16delinsAT MANE Select	NP_000292.1:n.2125+15_2125+16delinsAT