Canonical Allele Identifier: CA2695202311

Gene: MPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43349337_43349339delinsGCT , CM000663.2:g.43349337_43349339delinsGCT	GRCh38
NC_000001.10:g.43815008_43815010delinsGCT , CM000663.1:g.43815008_43815010delinsGCT	GRCh37
NC_000001.9:g.43587595_43587597delinsGCT	NCBI36
NG_007525.1:g.16534_16536delinsGCT , LRG_510:g.16534_16536delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.1543_1545delinsGCT MANE Select	ENSP00000361548.3:p.Trp515Ala
ENST00000413998.7:c.1522_1524delinsGCT	ENSP00000414004.3:p.Trp508Ala
ENST00000638732.1:n.1543_1545delinsGCT
ENST00000643351.1:c.75_77delinsGCT
ENST00000372470.7:c.1543_1545delinsGCT	ENSP00000361548.3:p.Trp515Ala
ENST00000413998.6:c.1543_1545delinsGCT	ENSP00000414004.2:p.Trp515Ala
ENST00000612993.1:c.1543_1545delinsGCT	ENSP00000480273.1:p.Trp515Ala
NM_005373.2:c.1543_1545delinsGCT , LRG_510t1:c.1543_1545delinsGCT	NP_005364.1:p.Trp515Ala
XM_011541478.1:c.1522_1524delinsGCT	XP_011539780.1:p.Trp508Ala
XM_017001320.1:c.1714_1716delinsGCT	XP_016856809.1:p.Trp572Ala
NM_005373.3:c.1543_1545delinsGCT MANE Select	NP_005364.1:p.Trp515Ala