Canonical Allele Identifier: CA339974109

Gene: MPL

Linked Data

• gnomAD v4: 1-43338715-G-C
• MyVariant Identifiers: chr1:g.43804386G>C (hg19) ; chr1:g.43338715G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338715G>C , CM000663.2:g.43338715G>C	GRCh38
NC_000001.10:g.43804386G>C , CM000663.1:g.43804386G>C	GRCh37
NC_000001.9:g.43576973G>C	NCBI36
NG_007525.1:g.5912G>C , LRG_510:g.5912G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.386G>C MANE Select	ENSP00000361548.3:p.Ser129Thr
ENST00000413998.7:c.365G>C	ENSP00000414004.3:p.Ser122Thr
ENST00000638732.1:n.386G>C
ENST00000372470.7:c.386G>C	ENSP00000361548.3:p.Ser129Thr
ENST00000413998.6:c.386G>C	ENSP00000414004.2:p.Ser129Thr
ENST00000612993.1:c.386G>C	ENSP00000480273.1:p.Ser129Thr
NM_005373.2:c.386G>C , LRG_510t1:c.386G>C	NP_005364.1:p.Ser129Thr
XM_011541478.1:c.365G>C	XP_011539780.1:p.Ser122Thr
XM_017001320.1:c.557G>C	XP_016856809.1:p.Ser186Thr
NM_005373.3:c.386G>C MANE Select	NP_005364.1:p.Ser129Thr