Canonical Allele Identifier: CA339973439

Gene: MPL

Linked Data

• MyVariant Identifiers: chr1:g.43804272A>C (hg19) ; chr1:g.43338601A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338601A>C , CM000663.2:g.43338601A>C	GRCh38
NC_000001.10:g.43804272A>C , CM000663.1:g.43804272A>C	GRCh37
NC_000001.9:g.43576859A>C	NCBI36
NG_007525.1:g.5798A>C , LRG_510:g.5798A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.272A>C MANE Select	ENSP00000361548.3:p.Tyr91Ser
ENST00000413998.7:c.251A>C	ENSP00000414004.3:p.Tyr84Ser
ENST00000638732.1:n.272A>C
ENST00000372470.7:c.272A>C	ENSP00000361548.3:p.Tyr91Ser
ENST00000413998.6:c.272A>C	ENSP00000414004.2:p.Tyr91Ser
ENST00000612993.1:c.272A>C	ENSP00000480273.1:p.Tyr91Ser
NM_005373.2:c.272A>C , LRG_510t1:c.272A>C	NP_005364.1:p.Tyr91Ser
XM_011541478.1:c.251A>C	XP_011539780.1:p.Tyr84Ser
XM_017001320.1:c.443A>C	XP_016856809.1:p.Tyr148Ser
NM_005373.3:c.272A>C MANE Select	NP_005364.1:p.Tyr91Ser