Canonical Allele Identifier: CA143772

Gene: MYPN

Linked Data

• ClinVar Variation Id: 31816
• ClinVar RCV Id: RCV000024509 ; RCV000043547
• dbSNP Id: rs199476408
• MyVariant Identifiers: chr10:g.69925560C>T (hg19) ; chr10:g.68165803C>T (hg38)
• PubMed: PMID:22286171

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.760C>T	ENSP00000346369.2:p.Gln254Ter
ENST00000373675.4:c.1585C>T	ENSP00000362779.4:p.Gln529Ter
ENST00000540630.6:c.1639C>T	ENSP00000441668.3:p.Gln547Ter
ENST00000613327.5:c.1585C>T	ENSP00000480757.2:p.Gln529Ter
ENST00000687572.1:c.463C>T	ENSP00000510427.1:p.Gln155Ter
ENST00000687705.1:c.*1834C>T	ENSP00000509639.1:n.*1834C>T
ENST00000688812.1:c.1561C>T	ENSP00000510658.1:p.Gln521Ter
ENST00000689002.1:n.637C>T
ENST00000690544.1:c.*856C>T	ENSP00000508989.1:n.*856C>T
ENST00000358913.10:c.1585C>T MANE Select	ENSP00000351790.5:p.Gln529Ter
ENST00000354393.6:c.760C>T	ENSP00000346369.2:p.Gln254Ter
ENST00000358913.9:c.1585C>T	ENSP00000351790.5:p.Gln529Ter
ENST00000540630.5:c.1585C>T	ENSP00000441668.2:p.Gln529Ter
ENST00000613327.4:c.703C>T	ENSP00000480757.1:p.Gln235Ter
NM_001256267.1:c.1585C>T	NP_001243196.1:p.Gln529Ter
NM_001256268.1:c.703C>T	NP_001243197.1:p.Gln235Ter
NM_032578.3:c.1585C>T , LRG_410t1:c.1585C>T	NP_115967.2:p.Gln529Ter
NR_045662.3:n.1012C>T
NR_045663.3:n.1853C>T
XM_006718043.2:c.1639C>T	XP_006718106.1:p.Gln547Ter
XM_011540292.1:c.1615C>T	XP_011538594.1:p.Gln539Ter
XM_017016833.1:c.1663C>T	XP_016872322.1:p.Gln555Ter
XM_017016834.2:c.1585C>T	XP_016872323.1:p.Gln529Ter
XM_024448236.1:c.463C>T	XP_024304004.1:p.Gln155Ter
NR_045662.4:n.1122C>T
NR_045663.4:n.1798C>T
NM_001256267.2:c.1585C>T	NP_001243196.1:p.Gln529Ter
NM_001256268.2:c.703C>T	NP_001243197.1:p.Gln235Ter
NM_032578.4:c.1585C>T MANE Select	NP_115967.2:p.Gln529Ter