Canonical Allele Identifier: CA376859202

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199469C>A , CM000672.2:g.68199469C>A	GRCh38
NC_000010.10:g.69959226C>A , CM000672.1:g.69959226C>A	GRCh37
NC_000010.9:g.69629232C>A	NCBI36
NG_032118.1:g.98353C>A , LRG_410:g.98353C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3387C>A MANE Select	NP_115967.2:p.His1129Gln
ENST00000358913.10:c.3387C>A MANE Select	ENSP00000351790.5:p.His1129Gln
NM_001256267.1:c.3387C>A	NP_001243196.1:p.His1129Gln
NM_001256267.2:c.3387C>A	NP_001243196.1:p.His1129Gln
NM_001256268.1:c.2505C>A	NP_001243197.1:p.His835Gln
NM_001256268.2:c.2505C>A	NP_001243197.1:p.His835Gln
NM_032578.3:c.3387C>A , LRG_410t1:c.3387C>A	NP_115967.2:p.His1129Gln
NR_045662.3:n.2814C>A
NR_045662.4:n.2924C>A
NR_045663.3:n.3516C>A
NR_045663.4:n.3461C>A
ENST00000354393.6:c.2562C>A	ENSP00000346369.2:p.His854Gln
ENST00000354393.7:c.2562C>A	ENSP00000346369.2:p.His854Gln
ENST00000358913.9:c.3387C>A	ENSP00000351790.5:p.His1129Gln
ENST00000540630.5:c.3387C>A	ENSP00000441668.2:p.His1129Gln
ENST00000540630.6:c.3441C>A	ENSP00000441668.3:p.His1147Gln
ENST00000613327.4:c.2505C>A	ENSP00000480757.1:p.His835Gln
ENST00000613327.5:c.3387C>A	ENSP00000480757.2:p.His1129Gln
ENST00000688812.1:c.*650C>A	ENSP00000510658.1:n.*650C>A
ENST00000690544.1:c.*2658C>A	ENSP00000508989.1:n.*2658C>A
XM_006718043.2:c.3441C>A	XP_006718106.1:p.His1147Gln
XM_011540292.1:c.3417C>A	XP_011538594.1:p.His1139Gln
XM_017016833.1:c.3465C>A	XP_016872322.1:p.His1155Gln
XM_017016834.2:c.3387C>A	XP_016872323.1:p.His1129Gln
XM_024448236.1:c.2265C>A	XP_024304004.1:p.His755Gln
XR_946029.1:n.1804-194G>T