Canonical Allele Identifier: CA1165575808
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337935_43337939delinsGCACA , CM000663.2:g.43337935_43337939delinsGCACA GRCh38
NC_000001.10:g.43803606_43803610delinsGCACA , CM000663.1:g.43803606_43803610delinsGCACA GRCh37
NC_000001.9:g.43576193_43576197delinsGCACA NCBI36
NG_007525.1:g.5132_5136delinsGCACA , LRG_510:g.5132_5136delinsGCACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.79+8_79+12delinsGCACA MANE Select ENSP00000361548.3:n.79+8_79+12delinsGCACA
ENST00000413998.7:c.79+8_79+12delinsGCACA ENSP00000414004.3:n.79+8_79+12delinsGCACA
ENST00000638732.1:n.79+8_79+12delinsGCACA
ENST00000372470.7:c.79+8_79+12delinsGCACA ENSP00000361548.3:n.79+8_79+12delinsGCACA
ENST00000413998.6:c.79+8_79+12delinsGCACA ENSP00000414004.2:n.79+8_79+12delinsGCACA
ENST00000612993.1:c.79+8_79+12delinsGCACA ENSP00000480273.1:n.79+8_79+12delinsGCACA
NM_005373.2:c.79+8_79+12delinsGCACA , LRG_510t1:c.79+8_79+12delinsGCACA NP_005364.1:n.79+8_79+12delinsGCACA
XM_011541478.1:c.79+8_79+12delinsGCACA XP_011539780.1:n.79+8_79+12delinsGCACA
XM_017001320.1:c.87_91delinsGCACA XP_016856809.1:p.Val29=
NM_005373.3:c.79+8_79+12delinsGCACA MANE Select NP_005364.1:n.79+8_79+12delinsGCACA