Canonical Allele Identifier: CA1141580752
Community Standard Title: NM_005373.3(MPL):c.1544G= (p.Trp515=)
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349338G= , CM000663.2:g.43349338G= GRCh38
NC_000001.10:g.43815009G= , CM000663.1:g.43815009G= GRCh37
NC_000001.9:g.43587596G= NCBI36
NG_007525.1:g.16535G= , LRG_510:g.16535G=

Transcript Alleles

HGVS Amino-acid Change
NM_005373.3:c.1544G= MANE Select NP_005364.1:p.Trp515=
ENST00000372470.9:c.1544G= MANE Select ENSP00000361548.3:p.Trp515=
NM_005373.2:c.1544G= , LRG_510t1:c.1544G= NP_005364.1:p.Trp515=
ENST00000372470.7:c.1544G= ENSP00000361548.3:p.Trp515=
ENST00000413998.6:c.1544G= ENSP00000414004.2:p.Trp515=
ENST00000413998.7:c.1523G= ENSP00000414004.3:p.Trp508=
ENST00000612993.1:c.1544G= ENSP00000480273.1:p.Trp515=
ENST00000638732.1:n.1544G=
ENST00000643351.1:c.76G=
XM_011541478.1:c.1523G= XP_011539780.1:p.Trp508=
XM_017001320.1:c.1715G= XP_016856809.1:p.Trp572=