Canonical Allele Identifier: CA376838484

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69925560C>A (hg19) ; chr10:g.68165803C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165803C>A , CM000672.2:g.68165803C>A	GRCh38
NC_000010.10:g.69925560C>A , CM000672.1:g.69925560C>A	GRCh37
NC_000010.9:g.69595566C>A	NCBI36
NG_032118.1:g.64687C>A , LRG_410:g.64687C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.760C>A	ENSP00000346369.2:p.Gln254Lys
ENST00000373675.4:c.1585C>A	ENSP00000362779.4:p.Gln529Lys
ENST00000540630.6:c.1639C>A	ENSP00000441668.3:p.Gln547Lys
ENST00000613327.5:c.1585C>A	ENSP00000480757.2:p.Gln529Lys
ENST00000687572.1:c.463C>A	ENSP00000510427.1:p.Gln155Lys
ENST00000687705.1:c.*1834C>A	ENSP00000509639.1:n.*1834C>A
ENST00000688812.1:c.1561C>A	ENSP00000510658.1:p.Gln521Lys
ENST00000689002.1:n.637C>A
ENST00000690544.1:c.*856C>A	ENSP00000508989.1:n.*856C>A
ENST00000358913.10:c.1585C>A MANE Select	ENSP00000351790.5:p.Gln529Lys
ENST00000354393.6:c.760C>A	ENSP00000346369.2:p.Gln254Lys
ENST00000358913.9:c.1585C>A	ENSP00000351790.5:p.Gln529Lys
ENST00000540630.5:c.1585C>A	ENSP00000441668.2:p.Gln529Lys
ENST00000613327.4:c.703C>A	ENSP00000480757.1:p.Gln235Lys
NM_001256267.1:c.1585C>A	NP_001243196.1:p.Gln529Lys
NM_001256268.1:c.703C>A	NP_001243197.1:p.Gln235Lys
NM_032578.3:c.1585C>A , LRG_410t1:c.1585C>A	NP_115967.2:p.Gln529Lys
NR_045662.3:n.1012C>A
NR_045663.3:n.1853C>A
XM_006718043.2:c.1639C>A	XP_006718106.1:p.Gln547Lys
XM_011540292.1:c.1615C>A	XP_011538594.1:p.Gln539Lys
XM_017016833.1:c.1663C>A	XP_016872322.1:p.Gln555Lys
XM_017016834.2:c.1585C>A	XP_016872323.1:p.Gln529Lys
XM_024448236.1:c.463C>A	XP_024304004.1:p.Gln155Lys
NR_045662.4:n.1122C>A
NR_045663.4:n.1798C>A
NM_001256267.2:c.1585C>A	NP_001243196.1:p.Gln529Lys
NM_001256268.2:c.703C>A	NP_001243197.1:p.Gln235Lys
NM_032578.4:c.1585C>A MANE Select	NP_115967.2:p.Gln529Lys