Canonical Allele Identifier: CA4087317

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160706556C>A , CM000668.2:g.160706556C>A	GRCh38
NC_000006.11:g.161127588C>A , CM000668.1:g.161127588C>A	GRCh37
NC_000006.10:g.161047578C>A	NCBI36
NG_016200.1:g.9364C>A , LRG_571:g.9364C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000301.5:c.185+14C>A MANE Select	NP_000292.1:n.185+14C>A
ENST00000308192.14:c.185+14C>A MANE Select	ENSP00000308938.9:n.185+14C>A
NM_000301.3:c.185+14C>A , LRG_571t1:c.185+14C>A	NP_000292.1:n.185+14C>A
NM_000301.4:c.185+14C>A	NP_000292.1:n.185+14C>A
NM_001168338.1:c.185+14C>A , LRG_571t2:c.185+14C>A	NP_001161810.1:n.185+14C>A
ENST00000297289.8:n.94+4203C>A
ENST00000297289.9:c.49+4203C>A	ENSP00000516619.1:n.49+4203C>A
ENST00000308192.13:c.185+14C>A	ENSP00000308938.9:n.185+14C>A
ENST00000366924.6:c.185+14C>A	ENSP00000355891.2:n.185+14C>A
ENST00000418964.1:c.199C>A	ENSP00000389424.1:p.Arg67Ser
ENST00000418964.2:c.199C>A	ENSP00000389424.2:p.Arg67Ser
ENST00000462918.5:n.222+14C>A
ENST00000471691.1:n.168+14C>A
ENST00000483038.5:n.198+14C>A
ENST00000484367.5:n.1155+14C>A
ENST00000494325.1:n.169+14C>A
ENST00000494325.2:c.-41+14C>A	ENSP00000516620.1:n.-41+14C>A
ENST00000706906.1:c.185+14C>A	ENSP00000516618.1:n.185+14C>A