Canonical Allele Identifier: CA1165575972
Gene: MPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338371G= , CM000663.2:g.43338371G= GRCh38
NC_000001.10:g.43804042G= , CM000663.1:g.43804042G= GRCh37
NC_000001.9:g.43576629G= NCBI36
NG_007525.1:g.5568G= , LRG_510:g.5568G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.212+140G= MANE Select ENSP00000361548.3:n.212+140G=
ENST00000413998.7:c.191+140G= ENSP00000414004.3:n.191+140G=
ENST00000638732.1:n.212+140G=
ENST00000372470.7:c.212+140G= ENSP00000361548.3:n.212+140G=
ENST00000413998.6:c.212+140G= ENSP00000414004.2:n.212+140G=
ENST00000612993.1:c.212+140G= ENSP00000480273.1:n.212+140G=
NM_005373.2:c.212+140G= , LRG_510t1:c.212+140G= NP_005364.1:n.212+140G=
XM_011541478.1:c.191+140G= XP_011539780.1:n.191+140G=
XM_017001320.1:c.383+140G= XP_016856809.1:n.383+140G=
NM_005373.3:c.212+140G= MANE Select NP_005364.1:n.212+140G=
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