Canonical Allele Identifier: CA1165575866
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338061_43338062delinsTG , CM000663.2:g.43338061_43338062delinsTG GRCh38
NC_000001.10:g.43803732_43803733delinsTG , CM000663.1:g.43803732_43803733delinsTG GRCh37
NC_000001.9:g.43576319_43576320delinsTG NCBI36
NG_007525.1:g.5258_5259delinsTG , LRG_510:g.5258_5259delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000372470.9:c.80-38_80-37delinsTG MANE Select ENSP00000361548.3:n.80-38_80-37delinsTG
ENST00000413998.7:c.80-59_80-58delinsTG ENSP00000414004.3:n.80-59_80-58delinsTG
ENST00000638732.1:n.80-38_80-37delinsTG
ENST00000372470.7:c.80-38_80-37delinsTG ENSP00000361548.3:n.80-38_80-37delinsTG
ENST00000413998.6:c.80-38_80-37delinsTG ENSP00000414004.2:n.80-38_80-37delinsTG
ENST00000612993.1:c.80-38_80-37delinsTG ENSP00000480273.1:n.80-38_80-37delinsTG
NM_005373.2:c.80-38_80-37delinsTG , LRG_510t1:c.80-38_80-37delinsTG NP_005364.1:n.80-38_80-37delinsTG
XM_011541478.1:c.80-59_80-58delinsTG XP_011539780.1:n.80-59_80-58delinsTG
XM_017001320.1:c.213_214delinsTG XP_016856809.1:p.Pro71=
NM_005373.3:c.80-38_80-37delinsTG MANE Select NP_005364.1:n.80-38_80-37delinsTG