Canonical Allele Identifier: CA1677205944

Gene: PLG

Linked Data

• dbSNP Id: rs1778188400
• gnomAD v4: 6-160741226-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741226G>C , CM000668.2:g.160741226G>C	GRCh38
NC_000006.11:g.161162258G>C , CM000668.1:g.161162258G>C	GRCh37
NC_000006.10:g.161082248G>C	NCBI36
NG_016200.1:g.44034G>C , LRG_571:g.44034G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297289.9:c.972-85G>C	ENSP00000516619.1:n.972-85G>C
ENST00000418964.2:c.2070-85G>C	ENSP00000389424.2:n.2070-85G>C
ENST00000706906.1:c.*2039-85G>C	ENSP00000516618.1:n.*2039-85G>C
ENST00000308192.14:c.2019-85G>C MANE Select	ENSP00000308938.9:n.2019-85G>C
ENST00000308192.13:c.2019-85G>C	ENSP00000308938.9:n.2019-85G>C
ENST00000461414.2:n.42-85G>C
ENST00000467466.1:n.320-85G>C
NM_000301.3:c.2019-85G>C , LRG_571t1:c.2019-85G>C	NP_000292.1:n.2019-85G>C
NM_000301.4:c.2019-85G>C	NP_000292.1:n.2019-85G>C
NM_000301.5:c.2019-85G>C MANE Select	NP_000292.1:n.2019-85G>C