Canonical Allele Identifier: CA417416575
Community Standard Title: NM_005373.3(MPL):c.96A>G (p.Ala32=)
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338115A>G , CM000663.2:g.43338115A>G GRCh38
NC_000001.10:g.43803786A>G , CM000663.1:g.43803786A>G GRCh37
NC_000001.9:g.43576373A>G NCBI36
NG_007525.1:g.5312A>G , LRG_510:g.5312A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005373.3:c.96A>G MANE Select NP_005364.1:p.Ala32=
ENST00000372470.9:c.96A>G MANE Select ENSP00000361548.3:p.Ala32=
NM_005373.2:c.96A>G , LRG_510t1:c.96A>G NP_005364.1:p.Ala32=
ENST00000372470.7:c.96A>G ENSP00000361548.3:p.Ala32=
ENST00000413998.6:c.96A>G ENSP00000414004.2:p.Ala32=
ENST00000413998.7:c.80-5A>G ENSP00000414004.3:n.80-5A>G
ENST00000612993.1:c.96A>G ENSP00000480273.1:p.Ala32=
ENST00000638732.1:n.96A>G
XM_011541478.1:c.80-5A>G XP_011539780.1:n.80-5A>G
XM_017001320.1:c.267A>G XP_016856809.1:p.Ala89=