Canonical Allele Identifier: CA1165579918
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349270C= , CM000663.2:g.43349270C= GRCh38
NC_000001.10:g.43814941C= , CM000663.1:g.43814941C= GRCh37
NC_000001.9:g.43587528C= NCBI36
NG_007525.1:g.16467C= , LRG_510:g.16467C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1476C= MANE Select ENSP00000361548.3:p.Ile492=
ENST00000413998.7:c.1455C= ENSP00000414004.3:p.Ile485=
ENST00000638732.1:n.1476C=
ENST00000643351.1:c.8C=
ENST00000372470.7:c.1476C= ENSP00000361548.3:p.Ile492=
ENST00000413998.6:c.1476C= ENSP00000414004.2:p.Ile492=
ENST00000612993.1:c.1476C= ENSP00000480273.1:p.Ile492=
NM_005373.2:c.1476C= , LRG_510t1:c.1476C= NP_005364.1:p.Ile492=
XM_011541478.1:c.1455C= XP_011539780.1:p.Ile485=
XM_017001320.1:c.1647C= XP_016856809.1:p.Ile549=
NM_005373.3:c.1476C= MANE Select NP_005364.1:p.Ile492=