Canonical Allele Identifier: CA1165575998

Gene: MPL

Linked Data

• dbSNP Id: rs1570464527
• gnomAD v4: 1-43338410-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338410T>C , CM000663.2:g.43338410T>C	GRCh38
NC_000001.10:g.43804081T>C , CM000663.1:g.43804081T>C	GRCh37
NC_000001.9:g.43576668T>C	NCBI36
NG_007525.1:g.5607T>C , LRG_510:g.5607T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.213-132T>C MANE Select	ENSP00000361548.3:n.213-132T>C
ENST00000413998.7:c.192-132T>C	ENSP00000414004.3:n.192-132T>C
ENST00000638732.1:n.213-132T>C
ENST00000372470.7:c.213-132T>C	ENSP00000361548.3:n.213-132T>C
ENST00000413998.6:c.213-132T>C	ENSP00000414004.2:n.213-132T>C
ENST00000612993.1:c.213-132T>C	ENSP00000480273.1:n.213-132T>C
NM_005373.2:c.213-132T>C , LRG_510t1:c.213-132T>C	NP_005364.1:n.213-132T>C
XM_011541478.1:c.192-132T>C	XP_011539780.1:n.192-132T>C
XM_017001320.1:c.384-132T>C	XP_016856809.1:n.384-132T>C
NM_005373.3:c.213-132T>C MANE Select	NP_005364.1:n.213-132T>C