Canonical Allele Identifier: CA645528776
Gene: MPL HGNC NCBI

Linked Data

COSMIC: COSM28487

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349337_43349339delinsAAA , CM000663.2:g.43349337_43349339delinsAAA GRCh38
NC_000001.10:g.43815008_43815010delinsAAA , CM000663.1:g.43815008_43815010delinsAAA GRCh37
NC_000001.9:g.43587595_43587597delinsAAA NCBI36
NG_007525.1:g.16534_16536delinsAAA , LRG_510:g.16534_16536delinsAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1543_1545delinsAAA MANE Select ENSP00000361548.3:p.Trp515Lys
ENST00000413998.7:c.1522_1524delinsAAA ENSP00000414004.3:p.Trp508Lys
ENST00000638732.1:n.1543_1545delinsAAA
ENST00000643351.1:c.75_77delinsAAA
ENST00000372470.7:c.1543_1545delinsAAA ENSP00000361548.3:p.Trp515Lys
ENST00000413998.6:c.1543_1545delinsAAA ENSP00000414004.2:p.Trp515Lys
ENST00000612993.1:c.1543_1545delinsAAA ENSP00000480273.1:p.Trp515Lys
NM_005373.2:c.1543_1545delinsAAA , LRG_510t1:c.1543_1545delinsAAA NP_005364.1:p.Trp515Lys
XM_011541478.1:c.1522_1524delinsAAA XP_011539780.1:p.Trp508Lys
XM_017001320.1:c.1714_1716delinsAAA XP_016856809.1:p.Trp572Lys
NM_005373.3:c.1543_1545delinsAAA MANE Select NP_005364.1:p.Trp515Lys