Canonical Allele Identifier: CA339988569

Gene: MPL

Linked Data

• gnomAD v4: 1-43349379-G-T
• MyVariant Identifiers: chr1:g.43815050G>T (hg19) ; chr1:g.43349379G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43349379G>T , CM000663.2:g.43349379G>T	GRCh38
NC_000001.10:g.43815050G>T , CM000663.1:g.43815050G>T	GRCh37
NC_000001.9:g.43587637G>T	NCBI36
NG_007525.1:g.16576G>T , LRG_510:g.16576G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.1565+20G>T MANE Select	ENSP00000361548.3:n.1565+20G>T
ENST00000413998.7:c.1544+20G>T	ENSP00000414004.3:n.1544+20G>T
ENST00000638732.1:n.1585G>T
ENST00000643351.1:c.97+20G>T
ENST00000372470.7:c.1565+20G>T	ENSP00000361548.3:n.1565+20G>T
ENST00000413998.6:c.1585G>T	ENSP00000414004.2:p.Gly529Ter
ENST00000612993.1:c.1585G>T	ENSP00000480273.1:p.Gly529Ter
NM_005373.2:c.1565+20G>T , LRG_510t1:c.1565+20G>T	NP_005364.1:n.1565+20G>T
XM_011541478.1:c.1544+20G>T	XP_011539780.1:n.1544+20G>T
XM_017001320.1:c.1736+20G>T	XP_016856809.1:n.1736+20G>T
NM_005373.3:c.1565+20G>T MANE Select	NP_005364.1:n.1565+20G>T