Canonical Allele Identifier: CA4087394

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160711097A>G , CM000668.2:g.160711097A>G	GRCh38
NC_000006.11:g.161132129A>G , CM000668.1:g.161132129A>G	GRCh37
NC_000006.10:g.161052119A>G	NCBI36
NG_016200.1:g.13905A>G , LRG_571:g.13905A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000301.5:c.313A>G MANE Select	NP_000292.1:p.Thr105Ala
ENST00000308192.14:c.313A>G MANE Select	ENSP00000308938.9:p.Thr105Ala
NM_000301.3:c.313A>G , LRG_571t1:c.313A>G	NP_000292.1:p.Thr105Ala
NM_000301.4:c.313A>G	NP_000292.1:p.Thr105Ala
NM_001168338.1:c.313A>G , LRG_571t2:c.313A>G	NP_001161810.1:p.Thr105Ala
ENST00000297289.8:n.94+8744A>G
ENST00000297289.9:c.49+8744A>G	ENSP00000516619.1:n.49+8744A>G
ENST00000308192.13:c.313A>G	ENSP00000308938.9:p.Thr105Ala
ENST00000366924.6:c.313A>G	ENSP00000355891.2:p.Thr105Ala
ENST00000418964.1:c.364A>G	ENSP00000389424.1:p.Thr122Ala
ENST00000418964.2:c.364A>G	ENSP00000389424.2:p.Thr122Ala
ENST00000462918.5:n.350A>G
ENST00000484367.5:n.1283A>G
ENST00000494325.1:n.297A>G
ENST00000494325.2:c.88A>G	ENSP00000516620.1:p.Thr30Ala
ENST00000706906.1:c.313A>G	ENSP00000516618.1:p.Thr105Ala