Canonical Allele Identifier: CA376840618

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926332T>G (hg19) ; chr10:g.68166575T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166575T>G , CM000672.2:g.68166575T>G	GRCh38
NC_000010.10:g.69926332T>G , CM000672.1:g.69926332T>G	GRCh37
NC_000010.9:g.69596338T>G	NCBI36
NG_032118.1:g.65459T>G , LRG_410:g.65459T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1057T>G	ENSP00000346369.2:p.Phe353Val
ENST00000373675.4:c.1882T>G	ENSP00000362779.4:p.Phe628Val
ENST00000540630.6:c.1936T>G	ENSP00000441668.3:p.Phe646Val
ENST00000613327.5:c.1882T>G	ENSP00000480757.2:p.Phe628Val
ENST00000687572.1:c.760T>G	ENSP00000510427.1:p.Phe254Val
ENST00000688812.1:c.1858T>G	ENSP00000510658.1:p.Phe620Val
ENST00000690544.1:c.*1153T>G	ENSP00000508989.1:n.*1153T>G
ENST00000358913.10:c.1882T>G MANE Select	ENSP00000351790.5:p.Phe628Val
ENST00000354393.6:c.1057T>G	ENSP00000346369.2:p.Phe353Val
ENST00000358913.9:c.1882T>G	ENSP00000351790.5:p.Phe628Val
ENST00000540630.5:c.1882T>G	ENSP00000441668.2:p.Phe628Val
ENST00000613327.4:c.1000T>G	ENSP00000480757.1:p.Phe334Val
NM_001256267.1:c.1882T>G	NP_001243196.1:p.Phe628Val
NM_001256268.1:c.1000T>G	NP_001243197.1:p.Phe334Val
NM_032578.3:c.1882T>G , LRG_410t1:c.1882T>G	NP_115967.2:p.Phe628Val
NR_045662.3:n.1309T>G
NR_045663.3:n.2150T>G
XM_006718043.2:c.1936T>G	XP_006718106.1:p.Phe646Val
XM_011540292.1:c.1912T>G	XP_011538594.1:p.Phe638Val
XM_017016833.1:c.1960T>G	XP_016872322.1:p.Phe654Val
XM_017016834.2:c.1882T>G	XP_016872323.1:p.Phe628Val
XM_024448236.1:c.760T>G	XP_024304004.1:p.Phe254Val
NR_045662.4:n.1419T>G
NR_045663.4:n.2095T>G
NM_001256267.2:c.1882T>G	NP_001243196.1:p.Phe628Val
NM_001256268.2:c.1000T>G	NP_001243197.1:p.Phe334Val
NM_032578.4:c.1882T>G MANE Select	NP_115967.2:p.Phe628Val