Canonical Allele Identifier: CA5523033

Gene: MYPN

Linked Data

• ClinVar Variation Id: 1026688
• ClinVar RCV Id: RCV001327168 ; RCV004035232
• dbSNP Id: rs755783155
• ExAC: 10:69959225 A / G
• gnomAD v2: 10-69959225-A-G
• gnomAD v4: 10-68199468-A-G
• MyVariant Identifiers: chr10:g.69959225A>G (hg19) ; chr10:g.68199468A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199468A>G , CM000672.2:g.68199468A>G	GRCh38
NC_000010.10:g.69959225A>G , CM000672.1:g.69959225A>G	GRCh37
NC_000010.9:g.69629231A>G	NCBI36
NG_032118.1:g.98352A>G , LRG_410:g.98352A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2561A>G	ENSP00000346369.2:p.His854Arg
ENST00000540630.6:c.3440A>G	ENSP00000441668.3:p.His1147Arg
ENST00000613327.5:c.3386A>G	ENSP00000480757.2:p.His1129Arg
ENST00000688812.1:c.*649A>G	ENSP00000510658.1:n.*649A>G
ENST00000690544.1:c.*2657A>G	ENSP00000508989.1:n.*2657A>G
ENST00000358913.10:c.3386A>G MANE Select	ENSP00000351790.5:p.His1129Arg
ENST00000354393.6:c.2561A>G	ENSP00000346369.2:p.His854Arg
ENST00000358913.9:c.3386A>G	ENSP00000351790.5:p.His1129Arg
ENST00000540630.5:c.3386A>G	ENSP00000441668.2:p.His1129Arg
ENST00000613327.4:c.2504A>G	ENSP00000480757.1:p.His835Arg
NM_001256267.1:c.3386A>G	NP_001243196.1:p.His1129Arg
NM_001256268.1:c.2504A>G	NP_001243197.1:p.His835Arg
NM_032578.3:c.3386A>G , LRG_410t1:c.3386A>G	NP_115967.2:p.His1129Arg
NR_045662.3:n.2813A>G
NR_045663.3:n.3515A>G
XM_006718043.2:c.3440A>G	XP_006718106.1:p.His1147Arg
XM_011540292.1:c.3416A>G	XP_011538594.1:p.His1139Arg
XR_946029.1:n.1804-193T>C
XM_017016833.1:c.3464A>G	XP_016872322.1:p.His1155Arg
XM_017016834.2:c.3386A>G	XP_016872323.1:p.His1129Arg
XM_024448236.1:c.2264A>G	XP_024304004.1:p.His755Arg
NR_045662.4:n.2923A>G
NR_045663.4:n.3460A>G
NM_001256267.2:c.3386A>G	NP_001243196.1:p.His1129Arg
NM_001256268.2:c.2504A>G	NP_001243197.1:p.His835Arg
NM_032578.4:c.3386A>G MANE Select	NP_115967.2:p.His1129Arg