Canonical Allele Identifier: CA366366204

Gene: PLG

Linked Data

• MyVariant Identifiers: chr6:g.161162362A>C (hg19) ; chr6:g.160741330A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741330A>C , CM000668.2:g.160741330A>C	GRCh38
NC_000006.11:g.161162362A>C , CM000668.1:g.161162362A>C	GRCh37
NC_000006.10:g.161082352A>C	NCBI36
NG_016200.1:g.44138A>C , LRG_571:g.44138A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.991A>C	ENSP00000516619.1:p.Lys331Gln
ENST00000418964.2:c.2089A>C	ENSP00000389424.2:p.Lys697Gln
ENST00000706906.1:c.*2058A>C	ENSP00000516618.1:n.*2058A>C
ENST00000308192.14:c.2038A>C MANE Select	ENSP00000308938.9:p.Lys680Gln
ENST00000308192.13:c.2038A>C	ENSP00000308938.9:p.Lys680Gln
ENST00000461414.2:n.61A>C
ENST00000467466.1:n.339A>C
NM_000301.3:c.2038A>C , LRG_571t1:c.2038A>C	NP_000292.1:p.Lys680Gln
NM_000301.4:c.2038A>C	NP_000292.1:p.Lys680Gln
NM_000301.5:c.2038A>C MANE Select	NP_000292.1:p.Lys680Gln