Canonical Allele Identifier: CA1165575999

Gene: MPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338411_43338420delinsAATCCCACCT , CM000663.2:g.43338411_43338420delinsAATCCCACCT	GRCh38
NC_000001.10:g.43804082_43804091delinsAATCCCACCT , CM000663.1:g.43804082_43804091delinsAATCCCACCT	GRCh37
NC_000001.9:g.43576669_43576678delinsAATCCCACCT	NCBI36
NG_007525.1:g.5608_5617delinsAATCCCACCT , LRG_510:g.5608_5617delinsAATCCCACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.213-131_213-122delinsAATCCCACCT MANE Select	ENSP00000361548.3:n.213-131_213-122delinsAATCCCACCT
ENST00000413998.7:c.192-131_192-122delinsAATCCCACCT	ENSP00000414004.3:n.192-131_192-122delinsAATCCCACCT
ENST00000638732.1:n.213-131_213-122delinsAATCCCACCT
ENST00000372470.7:c.213-131_213-122delinsAATCCCACCT	ENSP00000361548.3:n.213-131_213-122delinsAATCCCACCT
ENST00000413998.6:c.213-131_213-122delinsAATCCCACCT	ENSP00000414004.2:n.213-131_213-122delinsAATCCCACCT
ENST00000612993.1:c.213-131_213-122delinsAATCCCACCT	ENSP00000480273.1:n.213-131_213-122delinsAATCCCACCT
NM_005373.2:c.213-131_213-122delinsAATCCCACCT , LRG_510t1:c.213-131_213-122delinsAATCCCACCT	NP_005364.1:n.213-131_213-122delinsAATCCCACCT
XM_011541478.1:c.192-131_192-122delinsAATCCCACCT	XP_011539780.1:n.192-131_192-122delinsAATCCCACCT
XM_017001320.1:c.384-131_384-122delinsAATCCCACCT	XP_016856809.1:n.384-131_384-122delinsAATCCCACCT
NM_005373.3:c.213-131_213-122delinsAATCCCACCT MANE Select	NP_005364.1:n.213-131_213-122delinsAATCCCACCT