Canonical Allele Identifier: CA2681092795

Gene: PLG

Linked Data

• gnomAD v4: 6-160741429-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741431del , CM000668.2:g.160741431del	GRCh38
NC_000006.11:g.161162463del , CM000668.1:g.161162463del	GRCh37
NC_000006.10:g.161082453del	NCBI36
NG_016200.1:g.44239del , LRG_571:g.44239del

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.1078+14del	ENSP00000516619.1:n.1078+14del
ENST00000418964.2:c.2176+14del	ENSP00000389424.2:n.2176+14del
ENST00000706906.1:c.*2145+14del	ENSP00000516618.1:n.*2145+14del
ENST00000308192.14:c.2125+14del MANE Select	ENSP00000308938.9:n.2125+14del
ENST00000308192.13:c.2125+14del	ENSP00000308938.9:n.2125+14del
ENST00000461414.2:n.99+63del
ENST00000467466.1:n.426+14del
NM_000301.3:c.2125+14del , LRG_571t1:c.2125+14del	NP_000292.1:n.2125+14del
NM_000301.4:c.2125+14del	NP_000292.1:n.2125+14del
NM_000301.5:c.2125+14del MANE Select	NP_000292.1:n.2125+14del