Canonical Allele Identifier: CA1096557278

Gene: PLG

Linked Data

• dbSNP Id: rs1778193508
• gnomAD v3: 6-160741426-A-T
• gnomAD v4: 6-160741426-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160741426A>T , CM000668.2:g.160741426A>T	GRCh38
NC_000006.11:g.161162458A>T , CM000668.1:g.161162458A>T	GRCh37
NC_000006.10:g.161082448A>T	NCBI36
NG_016200.1:g.44234A>T , LRG_571:g.44234A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000297289.9:c.1078+9A>T	ENSP00000516619.1:n.1078+9A>T
ENST00000418964.2:c.2176+9A>T	ENSP00000389424.2:n.2176+9A>T
ENST00000706906.1:c.*2145+9A>T	ENSP00000516618.1:n.*2145+9A>T
ENST00000308192.14:c.2125+9A>T MANE Select	ENSP00000308938.9:n.2125+9A>T
ENST00000308192.13:c.2125+9A>T	ENSP00000308938.9:n.2125+9A>T
ENST00000461414.2:n.99+58A>T
ENST00000467466.1:n.426+9A>T
NM_000301.3:c.2125+9A>T , LRG_571t1:c.2125+9A>T	NP_000292.1:n.2125+9A>T
NM_000301.4:c.2125+9A>T	NP_000292.1:n.2125+9A>T
NM_000301.5:c.2125+9A>T MANE Select	NP_000292.1:n.2125+9A>T