Canonical Allele Identifier: CA417417336

Gene: MPL

Linked Data

• ClinVar Variation Id: 2935988
• ClinVar RCV Id: RCV003796274
• MyVariant Identifiers: chr1:g.43804264A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338593A>T , CM000663.2:g.43338593A>T	GRCh38
NC_000001.10:g.43804264A>T , CM000663.1:g.43804264A>T	GRCh37
NC_000001.9:g.43576851A>T	NCBI36
NG_007525.1:g.5790A>T , LRG_510:g.5790A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.264A>T MANE Select	ENSP00000361548.3:p.Gly88=
ENST00000413998.7:c.243A>T	ENSP00000414004.3:p.Gly81=
ENST00000638732.1:n.264A>T
ENST00000372470.7:c.264A>T	ENSP00000361548.3:p.Gly88=
ENST00000413998.6:c.264A>T	ENSP00000414004.2:p.Gly88=
ENST00000612993.1:c.264A>T	ENSP00000480273.1:p.Gly88=
NM_005373.2:c.264A>T , LRG_510t1:c.264A>T	NP_005364.1:p.Gly88=
XM_011541478.1:c.243A>T	XP_011539780.1:p.Gly81=
XM_017001320.1:c.435A>T	XP_016856809.1:p.Gly145=
NM_005373.3:c.264A>T MANE Select	NP_005364.1:p.Gly88=