Canonical Allele Identifier: CA2645222546
Gene: MPL HGNC NCBI

Linked Data

gnomAD v4: 1-43338796-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338796G>A , CM000663.2:g.43338796G>A GRCh38
NC_000001.10:g.43804467G>A , CM000663.1:g.43804467G>A GRCh37
NC_000001.9:g.43577054G>A NCBI36
NG_007525.1:g.5993G>A , LRG_510:g.5993G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.391+76G>A MANE Select ENSP00000361548.3:n.391+76G>A
ENST00000413998.7:c.370+76G>A ENSP00000414004.3:n.370+76G>A
ENST00000638732.1:n.391+76G>A
ENST00000372470.7:c.391+76G>A ENSP00000361548.3:n.391+76G>A
ENST00000413998.6:c.391+76G>A ENSP00000414004.2:n.391+76G>A
ENST00000612993.1:c.391+76G>A ENSP00000480273.1:n.391+76G>A
NM_005373.2:c.391+76G>A , LRG_510t1:c.391+76G>A NP_005364.1:n.391+76G>A
XM_011541478.1:c.370+76G>A XP_011539780.1:n.370+76G>A
XM_017001320.1:c.562+76G>A XP_016856809.1:n.562+76G>A
NM_005373.3:c.391+76G>A MANE Select NP_005364.1:n.391+76G>A