Canonical Allele Identifier: CA339973985

Gene: MPL

Linked Data

• MyVariant Identifiers: chr1:g.43804368G>C (hg19) ; chr1:g.43338697G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338697G>C , CM000663.2:g.43338697G>C	GRCh38
NC_000001.10:g.43804368G>C , CM000663.1:g.43804368G>C	GRCh37
NC_000001.9:g.43576955G>C	NCBI36
NG_007525.1:g.5894G>C , LRG_510:g.5894G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.368G>C MANE Select	ENSP00000361548.3:p.Arg123Pro
ENST00000413998.7:c.347G>C	ENSP00000414004.3:p.Arg116Pro
ENST00000638732.1:n.368G>C
ENST00000372470.7:c.368G>C	ENSP00000361548.3:p.Arg123Pro
ENST00000413998.6:c.368G>C	ENSP00000414004.2:p.Arg123Pro
ENST00000612993.1:c.368G>C	ENSP00000480273.1:p.Arg123Pro
NM_005373.2:c.368G>C , LRG_510t1:c.368G>C	NP_005364.1:p.Arg123Pro
XM_011541478.1:c.347G>C	XP_011539780.1:p.Arg116Pro
XM_017001320.1:c.539G>C	XP_016856809.1:p.Arg180Pro
NM_005373.3:c.368G>C MANE Select	NP_005364.1:p.Arg123Pro