Canonical Allele Identifier: CA376859204

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959226C>G (hg19) ; chr10:g.68199469C>G (hg38)

Genomic Alleles

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

Transcript Alleles

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