Canonical Allele Identifier: CA891841755
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349305_43349306insG , CM000663.2:g.43349305_43349306insG GRCh38
NC_000001.10:g.43814976_43814977insG , CM000663.1:g.43814976_43814977insG GRCh37
NC_000001.9:g.43587563_43587564insG NCBI36
NG_007525.1:g.16502_16503insG , LRG_510:g.16502_16503insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1511_1512insG MANE Select ENSP00000361548.3:p.Ser505GlnfsTer?
ENST00000413998.7:c.1490_1491insG ENSP00000414004.3:p.Ser498GlnfsTer?
ENST00000638732.1:n.1511_1512insG
ENST00000643351.1:c.43_44insG
ENST00000372470.7:c.1511_1512insG ENSP00000361548.3:p.Ser505GlnfsTer?
ENST00000413998.6:c.1511_1512insG ENSP00000414004.2:p.Ser505GlnfsTer?
ENST00000612993.1:c.1511_1512insG ENSP00000480273.1:p.Ser505GlnfsTer?
NM_005373.2:c.1511_1512insG , LRG_510t1:c.1511_1512insG NP_005364.1:p.Ser505GlnfsTer?
XM_011541478.1:c.1490_1491insG XP_011539780.1:p.Ser498GlnfsTer?
XM_017001320.1:c.1682_1683insG XP_016856809.1:p.Ser562GlnfsTer?
NM_005373.3:c.1511_1512insG MANE Select NP_005364.1:p.Ser505GlnfsTer?