Canonical Allele Identifier: CA376838514

Gene: MYPN

Linked Data

• dbSNP Id: rs2043044589
• MyVariant Identifiers: chr10:g.69925567A>G (hg19) ; chr10:g.68165810A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165810A>G , CM000672.2:g.68165810A>G	GRCh38
NC_000010.10:g.69925567A>G , CM000672.1:g.69925567A>G	GRCh37
NC_000010.9:g.69595573A>G	NCBI36
NG_032118.1:g.64694A>G , LRG_410:g.64694A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.767A>G	ENSP00000346369.2:p.His256Arg
ENST00000373675.4:c.1592A>G	ENSP00000362779.4:p.His531Arg
ENST00000540630.6:c.1646A>G	ENSP00000441668.3:p.His549Arg
ENST00000613327.5:c.1592A>G	ENSP00000480757.2:p.His531Arg
ENST00000687572.1:c.470A>G	ENSP00000510427.1:p.His157Arg
ENST00000687705.1:c.*1841A>G	ENSP00000509639.1:n.*1841A>G
ENST00000688812.1:c.1568A>G	ENSP00000510658.1:p.His523Arg
ENST00000689002.1:n.644A>G
ENST00000690544.1:c.*863A>G	ENSP00000508989.1:n.*863A>G
ENST00000358913.10:c.1592A>G MANE Select	ENSP00000351790.5:p.His531Arg
ENST00000354393.6:c.767A>G	ENSP00000346369.2:p.His256Arg
ENST00000358913.9:c.1592A>G	ENSP00000351790.5:p.His531Arg
ENST00000540630.5:c.1592A>G	ENSP00000441668.2:p.His531Arg
ENST00000613327.4:c.710A>G	ENSP00000480757.1:p.His237Arg
NM_001256267.1:c.1592A>G	NP_001243196.1:p.His531Arg
NM_001256268.1:c.710A>G	NP_001243197.1:p.His237Arg
NM_032578.3:c.1592A>G , LRG_410t1:c.1592A>G	NP_115967.2:p.His531Arg
NR_045662.3:n.1019A>G
NR_045663.3:n.1860A>G
XM_006718043.2:c.1646A>G	XP_006718106.1:p.His549Arg
XM_011540292.1:c.1622A>G	XP_011538594.1:p.His541Arg
XM_017016833.1:c.1670A>G	XP_016872322.1:p.His557Arg
XM_017016834.2:c.1592A>G	XP_016872323.1:p.His531Arg
XM_024448236.1:c.470A>G	XP_024304004.1:p.His157Arg
NR_045662.4:n.1129A>G
NR_045663.4:n.1805A>G
NM_001256267.2:c.1592A>G	NP_001243196.1:p.His531Arg
NM_001256268.2:c.710A>G	NP_001243197.1:p.His237Arg
NM_032578.4:c.1592A>G MANE Select	NP_115967.2:p.His531Arg