Canonical Allele Identifier: CA2681092790

Gene: PLG

Linked Data

• gnomAD v4: 6-160741422-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741422G>A , CM000668.2:g.160741422G>A	GRCh38
NC_000006.11:g.161162454G>A , CM000668.1:g.161162454G>A	GRCh37
NC_000006.10:g.161082444G>A	NCBI36
NG_016200.1:g.44230G>A , LRG_571:g.44230G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.1078+5G>A	ENSP00000516619.1:n.1078+5G>A
ENST00000418964.2:c.2176+5G>A	ENSP00000389424.2:n.2176+5G>A
ENST00000706906.1:c.*2145+5G>A	ENSP00000516618.1:n.*2145+5G>A
ENST00000308192.14:c.2125+5G>A MANE Select	ENSP00000308938.9:n.2125+5G>A
ENST00000308192.13:c.2125+5G>A	ENSP00000308938.9:n.2125+5G>A
ENST00000461414.2:n.99+54G>A
ENST00000467466.1:n.426+5G>A
NM_000301.3:c.2125+5G>A , LRG_571t1:c.2125+5G>A	NP_000292.1:n.2125+5G>A
NM_000301.4:c.2125+5G>A	NP_000292.1:n.2125+5G>A
NM_000301.5:c.2125+5G>A MANE Select	NP_000292.1:n.2125+5G>A