Canonical Allele Identifier: CA1165575965
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1647008345

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338358del , CM000663.2:g.43338358del GRCh38
NC_000001.10:g.43804029del , CM000663.1:g.43804029del GRCh37
NC_000001.9:g.43576616del NCBI36
NG_007525.1:g.5555del , LRG_510:g.5555del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.212+127del MANE Select ENSP00000361548.3:n.212+127del
ENST00000413998.7:c.191+127del ENSP00000414004.3:n.191+127del
ENST00000638732.1:n.212+127del
ENST00000372470.7:c.212+127del ENSP00000361548.3:n.212+127del
ENST00000413998.6:c.212+127del ENSP00000414004.2:n.212+127del
ENST00000612993.1:c.212+127del ENSP00000480273.1:n.212+127del
NM_005373.2:c.212+127del , LRG_510t1:c.212+127del NP_005364.1:n.212+127del
XM_011541478.1:c.191+127del XP_011539780.1:n.191+127del
XM_017001320.1:c.383+127del XP_016856809.1:n.383+127del
NM_005373.3:c.212+127del MANE Select NP_005364.1:n.212+127del