Canonical Allele Identifier: CA1165576009
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338432_43338434delinsTGA , CM000663.2:g.43338432_43338434delinsTGA GRCh38
NC_000001.10:g.43804103_43804105delinsTGA , CM000663.1:g.43804103_43804105delinsTGA GRCh37
NC_000001.9:g.43576690_43576692delinsTGA NCBI36
NG_007525.1:g.5629_5631delinsTGA , LRG_510:g.5629_5631delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.213-110_213-108delinsTGA MANE Select ENSP00000361548.3:n.213-110_213-108delinsTGA
ENST00000413998.7:c.192-110_192-108delinsTGA ENSP00000414004.3:n.192-110_192-108delinsTGA
ENST00000638732.1:n.213-110_213-108delinsTGA
ENST00000372470.7:c.213-110_213-108delinsTGA ENSP00000361548.3:n.213-110_213-108delinsTGA
ENST00000413998.6:c.213-110_213-108delinsTGA ENSP00000414004.2:n.213-110_213-108delinsTGA
ENST00000612993.1:c.213-110_213-108delinsTGA ENSP00000480273.1:n.213-110_213-108delinsTGA
NM_005373.2:c.213-110_213-108delinsTGA , LRG_510t1:c.213-110_213-108delinsTGA NP_005364.1:n.213-110_213-108delinsTGA
XM_011541478.1:c.192-110_192-108delinsTGA XP_011539780.1:n.192-110_192-108delinsTGA
XM_017001320.1:c.384-110_384-108delinsTGA XP_016856809.1:n.384-110_384-108delinsTGA
NM_005373.3:c.213-110_213-108delinsTGA MANE Select NP_005364.1:n.213-110_213-108delinsTGA