Canonical Allele Identifier: CA1165576057
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338581G= , CM000663.2:g.43338581G= GRCh38
NC_000001.10:g.43804252G= , CM000663.1:g.43804252G= GRCh37
NC_000001.9:g.43576839G= NCBI36
NG_007525.1:g.5778G= , LRG_510:g.5778G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.252G= MANE Select ENSP00000361548.3:p.Met84=
ENST00000413998.7:c.231G= ENSP00000414004.3:p.Met77=
ENST00000638732.1:n.252G=
ENST00000372470.7:c.252G= ENSP00000361548.3:p.Met84=
ENST00000413998.6:c.252G= ENSP00000414004.2:p.Met84=
ENST00000612993.1:c.252G= ENSP00000480273.1:p.Met84=
NM_005373.2:c.252G= , LRG_510t1:c.252G= NP_005364.1:p.Met84=
XM_011541478.1:c.231G= XP_011539780.1:p.Met77=
XM_017001320.1:c.423G= XP_016856809.1:p.Met141=
NM_005373.3:c.252G= MANE Select NP_005364.1:p.Met84=