Canonical Allele Identifier: CA339973873
Gene: MPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338679A>T , CM000663.2:g.43338679A>T GRCh38
NC_000001.10:g.43804350A>T , CM000663.1:g.43804350A>T GRCh37
NC_000001.9:g.43576937A>T NCBI36
NG_007525.1:g.5876A>T , LRG_510:g.5876A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.350A>T MANE Select ENSP00000361548.3:p.Asn117Ile
ENST00000413998.7:c.329A>T ENSP00000414004.3:p.Asn110Ile
ENST00000638732.1:n.350A>T
ENST00000372470.7:c.350A>T ENSP00000361548.3:p.Asn117Ile
ENST00000413998.6:c.350A>T ENSP00000414004.2:p.Asn117Ile
ENST00000612993.1:c.350A>T ENSP00000480273.1:p.Asn117Ile
NM_005373.2:c.350A>T , LRG_510t1:c.350A>T NP_005364.1:p.Asn117Ile
XM_011541478.1:c.329A>T XP_011539780.1:p.Asn110Ile
XM_017001320.1:c.521A>T XP_016856809.1:p.Asn174Ile
NM_005373.3:c.350A>T MANE Select NP_005364.1:p.Asn117Ile