Canonical Allele Identifier: CA2580593915
Gene: PLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160716958G>T , CM000668.2:g.160716958G>T GRCh38
NC_000006.11:g.161137990G>T , CM000668.1:g.161137990G>T GRCh37
NC_000006.10:g.161057980G>T NCBI36
NG_016200.1:g.19766G>T , LRG_571:g.19766G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297289.9:c.50-5450G>T ENSP00000516619.1:n.50-5450G>T
ENST00000418964.2:c.838+195G>T ENSP00000389424.2:n.838+195G>T
ENST00000706906.1:c.787+195G>T ENSP00000516618.1:n.787+195G>T
ENST00000308192.14:c.787+195G>T MANE Select ENSP00000308938.9:n.787+195G>T
ENST00000297289.8:n.95-5450G>T
ENST00000308192.13:c.787+195G>T ENSP00000308938.9:n.787+195G>T
NM_000301.3:c.787+195G>T , LRG_571t1:c.787+195G>T NP_000292.1:n.787+195G>T
NM_000301.4:c.787+195G>T NP_000292.1:n.787+195G>T
NM_000301.5:c.787+195G>T MANE Select NP_000292.1:n.787+195G>T