Canonical Allele Identifier: CA1165579935
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349279G= , CM000663.2:g.43349279G= GRCh38
NC_000001.10:g.43814950G= , CM000663.1:g.43814950G= GRCh37
NC_000001.9:g.43587537G= NCBI36
NG_007525.1:g.16476G= , LRG_510:g.16476G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1485G= MANE Select ENSP00000361548.3:p.Val495=
ENST00000413998.7:c.1464G= ENSP00000414004.3:p.Val488=
ENST00000638732.1:n.1485G=
ENST00000643351.1:c.17G=
ENST00000372470.7:c.1485G= ENSP00000361548.3:p.Val495=
ENST00000413998.6:c.1485G= ENSP00000414004.2:p.Val495=
ENST00000612993.1:c.1485G= ENSP00000480273.1:p.Val495=
NM_005373.2:c.1485G= , LRG_510t1:c.1485G= NP_005364.1:p.Val495=
XM_011541478.1:c.1464G= XP_011539780.1:p.Val488=
XM_017001320.1:c.1656G= XP_016856809.1:p.Val552=
NM_005373.3:c.1485G= MANE Select NP_005364.1:p.Val495=