Canonical Allele Identifier: CA339982353
Community Standard Title: NM_005373.3(MPL):c.1166-1G>C
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43346791G>C , CM000663.2:g.43346791G>C GRCh38
NC_000001.10:g.43812462G>C , CM000663.1:g.43812462G>C GRCh37
NC_000001.9:g.43585049G>C NCBI36
NG_007525.1:g.13988G>C , LRG_510:g.13988G>C

Transcript Alleles

HGVS Amino-acid Change
NM_005373.3:c.1166-1G>C MANE Select NP_005364.1:n.1166-1G>C
ENST00000372470.9:c.1166-1G>C MANE Select ENSP00000361548.3:n.1166-1G>C
NM_005373.2:c.1166-1G>C , LRG_510t1:c.1166-1G>C NP_005364.1:n.1166-1G>C
ENST00000372470.7:c.1166-1G>C ENSP00000361548.3:n.1166-1G>C
ENST00000413998.6:c.1166-1G>C ENSP00000414004.2:n.1166-1G>C
ENST00000413998.7:c.1145-1G>C ENSP00000414004.3:n.1145-1G>C
ENST00000612993.1:c.1166-1G>C ENSP00000480273.1:n.1166-1G>C
ENST00000638732.1:n.1166-1G>C
XM_011541478.1:c.1145-1G>C XP_011539780.1:n.1145-1G>C
XM_017001320.1:c.1337-1G>C XP_016856809.1:n.1337-1G>C