Canonical Allele Identifier: CA2743377648
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338743C>T , CM000663.2:g.43338743C>T GRCh38
NC_000001.10:g.43804414C>T , CM000663.1:g.43804414C>T GRCh37
NC_000001.9:g.43577001C>T NCBI36
NG_007525.1:g.5940C>T , LRG_510:g.5940C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.391+23C>T MANE Select ENSP00000361548.3:n.391+23C>T
ENST00000413998.7:c.370+23C>T ENSP00000414004.3:n.370+23C>T
ENST00000638732.1:n.391+23C>T
ENST00000372470.7:c.391+23C>T ENSP00000361548.3:n.391+23C>T
ENST00000413998.6:c.391+23C>T ENSP00000414004.2:n.391+23C>T
ENST00000612993.1:c.391+23C>T ENSP00000480273.1:n.391+23C>T
NM_005373.2:c.391+23C>T , LRG_510t1:c.391+23C>T NP_005364.1:n.391+23C>T
XM_011541478.1:c.370+23C>T XP_011539780.1:n.370+23C>T
XM_017001320.1:c.562+23C>T XP_016856809.1:n.562+23C>T
NM_005373.3:c.391+23C>T MANE Select NP_005364.1:n.391+23C>T