Canonical Allele Identifier: CA1165579952
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349295G= , CM000663.2:g.43349295G= GRCh38
NC_000001.10:g.43814966G= , CM000663.1:g.43814966G= GRCh37
NC_000001.9:g.43587553G= NCBI36
NG_007525.1:g.16492G= , LRG_510:g.16492G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1501G= MANE Select ENSP00000361548.3:p.Val501=
ENST00000413998.7:c.1480G= ENSP00000414004.3:p.Val494=
ENST00000638732.1:n.1501G=
ENST00000643351.1:c.33G=
ENST00000372470.7:c.1501G= ENSP00000361548.3:p.Val501=
ENST00000413998.6:c.1501G= ENSP00000414004.2:p.Val501=
ENST00000612993.1:c.1501G= ENSP00000480273.1:p.Val501=
NM_005373.2:c.1501G= , LRG_510t1:c.1501G= NP_005364.1:p.Val501=
XM_011541478.1:c.1480G= XP_011539780.1:p.Val494=
XM_017001320.1:c.1672G= XP_016856809.1:p.Val558=
NM_005373.3:c.1501G= MANE Select NP_005364.1:p.Val501=