Canonical Allele Identifier: CA339988389

Gene: MPL

Linked Data

• MyVariant Identifiers: chr1:g.43815033A>T (hg19) ; chr1:g.43349362A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43349362A>T , CM000663.2:g.43349362A>T	GRCh38
NC_000001.10:g.43815033A>T , CM000663.1:g.43815033A>T	GRCh37
NC_000001.9:g.43587620A>T	NCBI36
NG_007525.1:g.16559A>T , LRG_510:g.16559A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.1565+3A>T MANE Select	ENSP00000361548.3:n.1565+3A>T
ENST00000413998.7:c.1544+3A>T	ENSP00000414004.3:n.1544+3A>T
ENST00000638732.1:n.1568A>T
ENST00000643351.1:c.97+3A>T
ENST00000372470.7:c.1565+3A>T	ENSP00000361548.3:n.1565+3A>T
ENST00000413998.6:c.1568A>T	ENSP00000414004.2:p.Tyr523Phe
ENST00000612993.1:c.1568A>T	ENSP00000480273.1:p.Tyr523Phe
NM_005373.2:c.1565+3A>T , LRG_510t1:c.1565+3A>T	NP_005364.1:n.1565+3A>T
XM_011541478.1:c.1544+3A>T	XP_011539780.1:n.1544+3A>T
XM_017001320.1:c.1736+3A>T	XP_016856809.1:n.1736+3A>T
NM_005373.3:c.1565+3A>T MANE Select	NP_005364.1:n.1565+3A>T