Canonical Allele Identifier: CA366358207

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160707778G>C , CM000668.2:g.160707778G>C	GRCh38
NC_000006.11:g.161128810G>C , CM000668.1:g.161128810G>C	GRCh37
NC_000006.10:g.161048800G>C	NCBI36
NG_016200.1:g.10586G>C , LRG_571:g.10586G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000301.5:c.264G>C MANE Select	NP_000292.1:p.Met88Ile
ENST00000308192.14:c.264G>C MANE Select	ENSP00000308938.9:p.Met88Ile
NM_000301.3:c.264G>C , LRG_571t1:c.264G>C	NP_000292.1:p.Met88Ile
NM_000301.4:c.264G>C	NP_000292.1:p.Met88Ile
NM_001168338.1:c.264G>C , LRG_571t2:c.264G>C	NP_001161810.1:p.Met88Ile
ENST00000297289.8:n.94+5425G>C
ENST00000297289.9:c.49+5425G>C	ENSP00000516619.1:n.49+5425G>C
ENST00000308192.13:c.264G>C	ENSP00000308938.9:p.Met88Ile
ENST00000366924.6:c.264G>C	ENSP00000355891.2:p.Met88Ile
ENST00000418964.1:c.315G>C	ENSP00000389424.1:p.Met105Ile
ENST00000418964.2:c.315G>C	ENSP00000389424.2:p.Met105Ile
ENST00000462918.5:n.301G>C
ENST00000471691.1:n.247G>C
ENST00000483038.5:n.277G>C
ENST00000484367.5:n.1234G>C
ENST00000494325.1:n.248G>C
ENST00000494325.2:c.39G>C	ENSP00000516620.1:p.Met13Ile
ENST00000706906.1:c.264G>C	ENSP00000516618.1:p.Met88Ile