Canonical Allele Identifier: CA4087403

Gene: PLG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160711114C>T , CM000668.2:g.160711114C>T	GRCh38
NC_000006.11:g.161132146C>T , CM000668.1:g.161132146C>T	GRCh37
NC_000006.10:g.161052136C>T	NCBI36
NG_016200.1:g.13922C>T , LRG_571:g.13922C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000301.5:c.330C>T MANE Select	NP_000292.1:p.Asn110=
ENST00000308192.14:c.330C>T MANE Select	ENSP00000308938.9:p.Asn110=
NM_000301.3:c.330C>T , LRG_571t1:c.330C>T	NP_000292.1:p.Asn110=
NM_000301.4:c.330C>T	NP_000292.1:p.Asn110=
NM_001168338.1:c.330C>T , LRG_571t2:c.330C>T	NP_001161810.1:p.Asn110=
ENST00000297289.8:n.94+8761C>T
ENST00000297289.9:c.49+8761C>T	ENSP00000516619.1:n.49+8761C>T
ENST00000308192.13:c.330C>T	ENSP00000308938.9:p.Asn110=
ENST00000366924.6:c.330C>T	ENSP00000355891.2:p.Asn110=
ENST00000418964.1:c.381C>T	ENSP00000389424.1:p.Asn127=
ENST00000418964.2:c.381C>T	ENSP00000389424.2:p.Asn127=
ENST00000462918.5:n.367C>T
ENST00000484367.5:n.1300C>T
ENST00000494325.1:n.314C>T
ENST00000494325.2:c.105C>T	ENSP00000516620.1:p.Asn35=
ENST00000706906.1:c.330C>T	ENSP00000516618.1:p.Asn110=