Canonical Allele Identifier: CA376841177

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926423T>G (hg19) ; chr10:g.68166666T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166666T>G , CM000672.2:g.68166666T>G	GRCh38
NC_000010.10:g.69926423T>G , CM000672.1:g.69926423T>G	GRCh37
NC_000010.9:g.69596429T>G	NCBI36
NG_032118.1:g.65550T>G , LRG_410:g.65550T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1148T>G	ENSP00000346369.2:p.Leu383Arg
ENST00000373675.4:c.1973T>G	ENSP00000362779.4:p.Leu658Arg
ENST00000540630.6:c.2027T>G	ENSP00000441668.3:p.Leu676Arg
ENST00000613327.5:c.1973T>G	ENSP00000480757.2:p.Leu658Arg
ENST00000687572.1:c.851T>G
ENST00000688812.1:c.1949T>G	ENSP00000510658.1:p.Leu650Arg
ENST00000690544.1:c.*1244T>G	ENSP00000508989.1:n.*1244T>G
ENST00000358913.10:c.1973T>G MANE Select	ENSP00000351790.5:p.Leu658Arg
ENST00000354393.6:c.1148T>G	ENSP00000346369.2:p.Leu383Arg
ENST00000358913.9:c.1973T>G	ENSP00000351790.5:p.Leu658Arg
ENST00000540630.5:c.1973T>G	ENSP00000441668.2:p.Leu658Arg
ENST00000613327.4:c.1091T>G	ENSP00000480757.1:p.Leu364Arg
NM_001256267.1:c.1973T>G	NP_001243196.1:p.Leu658Arg
NM_001256268.1:c.1091T>G	NP_001243197.1:p.Leu364Arg
NM_032578.3:c.1973T>G , LRG_410t1:c.1973T>G	NP_115967.2:p.Leu658Arg
NR_045662.3:n.1400T>G
NR_045663.3:n.2241T>G
XM_006718043.2:c.2027T>G	XP_006718106.1:p.Leu676Arg
XM_011540292.1:c.2003T>G	XP_011538594.1:p.Leu668Arg
XM_017016833.1:c.2051T>G	XP_016872322.1:p.Leu684Arg
XM_017016834.2:c.1973T>G	XP_016872323.1:p.Leu658Arg
XM_024448236.1:c.851T>G	XP_024304004.1:p.Leu284Arg
NR_045662.4:n.1510T>G
NR_045663.4:n.2186T>G
NM_001256267.2:c.1973T>G	NP_001243196.1:p.Leu658Arg
NM_001256268.2:c.1091T>G	NP_001243197.1:p.Leu364Arg
NM_032578.4:c.1973T>G MANE Select	NP_115967.2:p.Leu658Arg