Canonical Allele Identifier: CA417428401
Gene: MPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.43818350T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43352679T>G , CM000663.2:g.43352679T>G GRCh38
NC_000001.10:g.43818350T>G , CM000663.1:g.43818350T>G GRCh37
NC_000001.9:g.43590937T>G NCBI36
NG_007525.1:g.19876T>G , LRG_510:g.19876T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372470.9:c.1815T>G MANE Select ENSP00000361548.3:p.Ser605=
ENST00000413998.7:c.1794T>G ENSP00000414004.3:p.Ser598=
ENST00000643351.1:c.473T>G
ENST00000372470.7:c.1815T>G ENSP00000361548.3:p.Ser605=
NM_005373.2:c.1815T>G , LRG_510t1:c.1815T>G NP_005364.1:p.Ser605=
XM_011541478.1:c.1794T>G XP_011539780.1:p.Ser598=
XM_017001320.1:c.1986T>G XP_016856809.1:p.Ser662=
NM_005373.3:c.1815T>G MANE Select NP_005364.1:p.Ser605=