Canonical Allele Identifier: CA376859194

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959224C>G (hg19) ; chr10:g.68199467C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199467C>G , CM000672.2:g.68199467C>G	GRCh38
NC_000010.10:g.69959224C>G , CM000672.1:g.69959224C>G	GRCh37
NC_000010.9:g.69629230C>G	NCBI36
NG_032118.1:g.98351C>G , LRG_410:g.98351C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2560C>G	ENSP00000346369.2:p.His854Asp
ENST00000540630.6:c.3439C>G	ENSP00000441668.3:p.His1147Asp
ENST00000613327.5:c.3385C>G	ENSP00000480757.2:p.His1129Asp
ENST00000688812.1:c.*648C>G	ENSP00000510658.1:n.*648C>G
ENST00000690544.1:c.*2656C>G	ENSP00000508989.1:n.*2656C>G
ENST00000358913.10:c.3385C>G MANE Select	ENSP00000351790.5:p.His1129Asp
ENST00000354393.6:c.2560C>G	ENSP00000346369.2:p.His854Asp
ENST00000358913.9:c.3385C>G	ENSP00000351790.5:p.His1129Asp
ENST00000540630.5:c.3385C>G	ENSP00000441668.2:p.His1129Asp
ENST00000613327.4:c.2503C>G	ENSP00000480757.1:p.His835Asp
NM_001256267.1:c.3385C>G	NP_001243196.1:p.His1129Asp
NM_001256268.1:c.2503C>G	NP_001243197.1:p.His835Asp
NM_032578.3:c.3385C>G , LRG_410t1:c.3385C>G	NP_115967.2:p.His1129Asp
NR_045662.3:n.2812C>G
NR_045663.3:n.3514C>G
XM_006718043.2:c.3439C>G	XP_006718106.1:p.His1147Asp
XM_011540292.1:c.3415C>G	XP_011538594.1:p.His1139Asp
XR_946029.1:n.1804-192G>C
XM_017016833.1:c.3463C>G	XP_016872322.1:p.His1155Asp
XM_017016834.2:c.3385C>G	XP_016872323.1:p.His1129Asp
XM_024448236.1:c.2263C>G	XP_024304004.1:p.His755Asp
NR_045662.4:n.2922C>G
NR_045663.4:n.3459C>G
NM_001256267.2:c.3385C>G	NP_001243196.1:p.His1129Asp
NM_001256268.2:c.2503C>G	NP_001243197.1:p.His835Asp
NM_032578.4:c.3385C>G MANE Select	NP_115967.2:p.His1129Asp