Canonical Allele Identifier: CA376837706

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69925473T>G (hg19) ; chr10:g.68165716T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165716T>G , CM000672.2:g.68165716T>G	GRCh38
NC_000010.10:g.69925473T>G , CM000672.1:g.69925473T>G	GRCh37
NC_000010.9:g.69595479T>G	NCBI36
NG_032118.1:g.64600T>G , LRG_410:g.64600T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.673T>G	ENSP00000346369.2:p.Leu225Val
ENST00000373675.4:c.1498T>G	ENSP00000362779.4:p.Leu500Val
ENST00000540630.6:c.1552T>G	ENSP00000441668.3:p.Leu518Val
ENST00000613327.5:c.1498T>G	ENSP00000480757.2:p.Leu500Val
ENST00000687572.1:c.376T>G	ENSP00000510427.1:p.Leu126Val
ENST00000687705.1:c.*1747T>G	ENSP00000509639.1:n.*1747T>G
ENST00000688812.1:c.1474T>G	ENSP00000510658.1:p.Leu492Val
ENST00000689002.1:n.550T>G
ENST00000690544.1:c.*769T>G	ENSP00000508989.1:n.*769T>G
ENST00000358913.10:c.1498T>G MANE Select	ENSP00000351790.5:p.Leu500Val
ENST00000354393.6:c.673T>G	ENSP00000346369.2:p.Leu225Val
ENST00000358913.9:c.1498T>G	ENSP00000351790.5:p.Leu500Val
ENST00000540630.5:c.1498T>G	ENSP00000441668.2:p.Leu500Val
ENST00000613327.4:c.616T>G	ENSP00000480757.1:p.Leu206Val
NM_001256267.1:c.1498T>G	NP_001243196.1:p.Leu500Val
NM_001256268.1:c.616T>G	NP_001243197.1:p.Leu206Val
NM_032578.3:c.1498T>G , LRG_410t1:c.1498T>G	NP_115967.2:p.Leu500Val
NR_045662.3:n.925T>G
NR_045663.3:n.1766T>G
XM_006718043.2:c.1552T>G	XP_006718106.1:p.Leu518Val
XM_011540292.1:c.1528T>G	XP_011538594.1:p.Leu510Val
XM_017016833.1:c.1576T>G	XP_016872322.1:p.Leu526Val
XM_017016834.2:c.1498T>G	XP_016872323.1:p.Leu500Val
XM_024448236.1:c.376T>G	XP_024304004.1:p.Leu126Val
NR_045662.4:n.1035T>G
NR_045663.4:n.1711T>G
NM_001256267.2:c.1498T>G	NP_001243196.1:p.Leu500Val
NM_001256268.2:c.616T>G	NP_001243197.1:p.Leu206Val
NM_032578.4:c.1498T>G MANE Select	NP_115967.2:p.Leu500Val