Canonical Allele Identifier: CA2645221965
Gene: MPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338322del , CM000663.2:g.43338322del GRCh38
NC_000001.10:g.43803993del , CM000663.1:g.43803993del GRCh37
NC_000001.9:g.43576580del NCBI36
NG_007525.1:g.5519del , LRG_510:g.5519del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.212+91del MANE Select ENSP00000361548.3:n.212+91del
ENST00000413998.7:c.191+91del ENSP00000414004.3:n.191+91del
ENST00000638732.1:n.212+91del
ENST00000372470.7:c.212+91del ENSP00000361548.3:n.212+91del
ENST00000413998.6:c.212+91del ENSP00000414004.2:n.212+91del
ENST00000612993.1:c.212+91del ENSP00000480273.1:n.212+91del
NM_005373.2:c.212+91del , LRG_510t1:c.212+91del NP_005364.1:n.212+91del
XM_011541478.1:c.191+91del XP_011539780.1:n.191+91del
XM_017001320.1:c.383+91del XP_016856809.1:n.383+91del
NM_005373.3:c.212+91del MANE Select NP_005364.1:n.212+91del