Canonical Allele Identifier: CA339987516

Gene: MPL

Linked Data

• dbSNP Id: rs2153919400
• MyVariant Identifiers: chr1:g.43814951A>T (hg19) ; chr1:g.43349280A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43349280A>T , CM000663.2:g.43349280A>T	GRCh38
NC_000001.10:g.43814951A>T , CM000663.1:g.43814951A>T	GRCh37
NC_000001.9:g.43587538A>T	NCBI36
NG_007525.1:g.16477A>T , LRG_510:g.16477A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.1486A>T MANE Select	ENSP00000361548.3:p.Thr496Ser
ENST00000413998.7:c.1465A>T	ENSP00000414004.3:p.Thr489Ser
ENST00000638732.1:n.1486A>T
ENST00000643351.1:c.18A>T
ENST00000372470.7:c.1486A>T	ENSP00000361548.3:p.Thr496Ser
ENST00000413998.6:c.1486A>T	ENSP00000414004.2:p.Thr496Ser
ENST00000612993.1:c.1486A>T	ENSP00000480273.1:p.Thr496Ser
NM_005373.2:c.1486A>T , LRG_510t1:c.1486A>T	NP_005364.1:p.Thr496Ser
XM_011541478.1:c.1465A>T	XP_011539780.1:p.Thr489Ser
XM_017001320.1:c.1657A>T	XP_016856809.1:p.Thr553Ser
NM_005373.3:c.1486A>T MANE Select	NP_005364.1:p.Thr496Ser