Canonical Allele Identifier: CA366366612

Gene: PLG

Linked Data

• MyVariant Identifiers: chr6:g.161162450G>T (hg19) ; chr6:g.160741418G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741418G>T , CM000668.2:g.160741418G>T	GRCh38
NC_000006.11:g.161162450G>T , CM000668.1:g.161162450G>T	GRCh37
NC_000006.10:g.161082440G>T	NCBI36
NG_016200.1:g.44226G>T , LRG_571:g.44226G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.1078+1G>T	ENSP00000516619.1:n.1078+1G>T
ENST00000418964.2:c.2176+1G>T	ENSP00000389424.2:n.2176+1G>T
ENST00000706906.1:c.*2145+1G>T	ENSP00000516618.1:n.*2145+1G>T
ENST00000308192.14:c.2125+1G>T MANE Select	ENSP00000308938.9:n.2125+1G>T
ENST00000308192.13:c.2125+1G>T	ENSP00000308938.9:n.2125+1G>T
ENST00000461414.2:n.99+50G>T
ENST00000467466.1:n.426+1G>T
NM_000301.3:c.2125+1G>T , LRG_571t1:c.2125+1G>T	NP_000292.1:n.2125+1G>T
NM_000301.4:c.2125+1G>T	NP_000292.1:n.2125+1G>T
NM_000301.5:c.2125+1G>T MANE Select	NP_000292.1:n.2125+1G>T