Canonical Allele Identifier: CA376839976

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926186A>T (hg19) ; chr10:g.68166429A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166429A>T , CM000672.2:g.68166429A>T	GRCh38
NC_000010.10:g.69926186A>T , CM000672.1:g.69926186A>T	GRCh37
NC_000010.9:g.69596192A>T	NCBI36
NG_032118.1:g.65313A>T , LRG_410:g.65313A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.911A>T	ENSP00000346369.2:p.Glu304Val
ENST00000373675.4:c.1736A>T	ENSP00000362779.4:p.Glu579Val
ENST00000540630.6:c.1790A>T	ENSP00000441668.3:p.Glu597Val
ENST00000613327.5:c.1736A>T	ENSP00000480757.2:p.Glu579Val
ENST00000687572.1:c.614A>T	ENSP00000510427.1:p.Glu205Val
ENST00000688812.1:c.1712A>T	ENSP00000510658.1:p.Glu571Val
ENST00000690544.1:c.*1007A>T	ENSP00000508989.1:n.*1007A>T
ENST00000358913.10:c.1736A>T MANE Select	ENSP00000351790.5:p.Glu579Val
ENST00000354393.6:c.911A>T	ENSP00000346369.2:p.Glu304Val
ENST00000358913.9:c.1736A>T	ENSP00000351790.5:p.Glu579Val
ENST00000540630.5:c.1736A>T	ENSP00000441668.2:p.Glu579Val
ENST00000613327.4:c.854A>T	ENSP00000480757.1:p.Glu285Val
NM_001256267.1:c.1736A>T	NP_001243196.1:p.Glu579Val
NM_001256268.1:c.854A>T	NP_001243197.1:p.Glu285Val
NM_032578.3:c.1736A>T , LRG_410t1:c.1736A>T	NP_115967.2:p.Glu579Val
NR_045662.3:n.1163A>T
NR_045663.3:n.2004A>T
XM_006718043.2:c.1790A>T	XP_006718106.1:p.Glu597Val
XM_011540292.1:c.1766A>T	XP_011538594.1:p.Glu589Val
XM_017016833.1:c.1814A>T	XP_016872322.1:p.Glu605Val
XM_017016834.2:c.1736A>T	XP_016872323.1:p.Glu579Val
XM_024448236.1:c.614A>T	XP_024304004.1:p.Glu205Val
NR_045662.4:n.1273A>T
NR_045663.4:n.1949A>T
NM_001256267.2:c.1736A>T	NP_001243196.1:p.Glu579Val
NM_001256268.2:c.854A>T	NP_001243197.1:p.Glu285Val
NM_032578.4:c.1736A>T MANE Select	NP_115967.2:p.Glu579Val