Canonical Allele Identifier: CA1165575947
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338313T= , CM000663.2:g.43338313T= GRCh38
NC_000001.10:g.43803984T= , CM000663.1:g.43803984T= GRCh37
NC_000001.9:g.43576571T= NCBI36
NG_007525.1:g.5510T= , LRG_510:g.5510T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.212+82T= MANE Select ENSP00000361548.3:n.212+82T=
ENST00000413998.7:c.191+82T= ENSP00000414004.3:n.191+82T=
ENST00000638732.1:n.212+82T=
ENST00000372470.7:c.212+82T= ENSP00000361548.3:n.212+82T=
ENST00000413998.6:c.212+82T= ENSP00000414004.2:n.212+82T=
ENST00000612993.1:c.212+82T= ENSP00000480273.1:n.212+82T=
NM_005373.2:c.212+82T= , LRG_510t1:c.212+82T= NP_005364.1:n.212+82T=
XM_011541478.1:c.191+82T= XP_011539780.1:n.191+82T=
XM_017001320.1:c.383+82T= XP_016856809.1:n.383+82T=
NM_005373.3:c.212+82T= MANE Select NP_005364.1:n.212+82T=