Canonical Allele Identifier: CA2578791001

Gene: PLG

Linked Data

• gnomAD v4: 6-160741437-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741437C>A , CM000668.2:g.160741437C>A	GRCh38
NC_000006.11:g.161162469C>A , CM000668.1:g.161162469C>A	GRCh37
NC_000006.10:g.161082459C>A	NCBI36
NG_016200.1:g.44245C>A , LRG_571:g.44245C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.1078+20C>A	ENSP00000516619.1:n.1078+20C>A
ENST00000418964.2:c.2176+20C>A	ENSP00000389424.2:n.2176+20C>A
ENST00000706906.1:c.*2145+20C>A	ENSP00000516618.1:n.*2145+20C>A
ENST00000308192.14:c.2125+20C>A MANE Select	ENSP00000308938.9:n.2125+20C>A
ENST00000308192.13:c.2125+20C>A	ENSP00000308938.9:n.2125+20C>A
ENST00000461414.2:n.99+69C>A
ENST00000467466.1:n.426+20C>A
NM_000301.3:c.2125+20C>A , LRG_571t1:c.2125+20C>A	NP_000292.1:n.2125+20C>A
NM_000301.4:c.2125+20C>A	NP_000292.1:n.2125+20C>A
NM_000301.5:c.2125+20C>A MANE Select	NP_000292.1:n.2125+20C>A