Canonical Allele Identifier: CA1165575948
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338315C= , CM000663.2:g.43338315C= GRCh38
NC_000001.10:g.43803986C= , CM000663.1:g.43803986C= GRCh37
NC_000001.9:g.43576573C= NCBI36
NG_007525.1:g.5512C= , LRG_510:g.5512C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.212+84C= MANE Select ENSP00000361548.3:n.212+84C=
ENST00000413998.7:c.191+84C= ENSP00000414004.3:n.191+84C=
ENST00000638732.1:n.212+84C=
ENST00000372470.7:c.212+84C= ENSP00000361548.3:n.212+84C=
ENST00000413998.6:c.212+84C= ENSP00000414004.2:n.212+84C=
ENST00000612993.1:c.212+84C= ENSP00000480273.1:n.212+84C=
NM_005373.2:c.212+84C= , LRG_510t1:c.212+84C= NP_005364.1:n.212+84C=
XM_011541478.1:c.191+84C= XP_011539780.1:n.191+84C=
XM_017001320.1:c.383+84C= XP_016856809.1:n.383+84C=
NM_005373.3:c.212+84C= MANE Select NP_005364.1:n.212+84C=