Canonical Allele Identifier: CA335270

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68174328A>G , CM000672.2:g.68174328A>G	GRCh38
NC_000010.10:g.69934085A>G , CM000672.1:g.69934085A>G	GRCh37
NC_000010.9:g.69604091A>G	NCBI36
NG_032118.1:g.73212A>G , LRG_410:g.73212A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1411A>G	ENSP00000346369.2:p.Thr471Ala
ENST00000540630.6:c.2290A>G	ENSP00000441668.3:p.Thr764Ala
ENST00000613327.5:c.2236A>G	ENSP00000480757.2:p.Thr746Ala
ENST00000688812.1:c.2212A>G	ENSP00000510658.1:p.Thr738Ala
ENST00000690544.1:c.*1507A>G	ENSP00000508989.1:n.*1507A>G
ENST00000358913.10:c.2236A>G MANE Select	ENSP00000351790.5:p.Thr746Ala
ENST00000354393.6:c.1411A>G	ENSP00000346369.2:p.Thr471Ala
ENST00000358913.9:c.2236A>G	ENSP00000351790.5:p.Thr746Ala
ENST00000540630.5:c.2236A>G	ENSP00000441668.2:p.Thr746Ala
ENST00000613327.4:c.1354A>G	ENSP00000480757.1:p.Thr452Ala
NM_001256267.1:c.2236A>G	NP_001243196.1:p.Thr746Ala
NM_001256268.1:c.1354A>G	NP_001243197.1:p.Thr452Ala
NM_032578.3:c.2236A>G , LRG_410t1:c.2236A>G	NP_115967.2:p.Thr746Ala
NR_045662.3:n.1663A>G
NR_045663.3:n.2504A>G
XM_006718043.2:c.2290A>G	XP_006718106.1:p.Thr764Ala
XM_011540292.1:c.2266A>G	XP_011538594.1:p.Thr756Ala
XM_017016833.1:c.2314A>G	XP_016872322.1:p.Thr772Ala
XM_017016834.2:c.2236A>G	XP_016872323.1:p.Thr746Ala
XM_024448236.1:c.1114A>G	XP_024304004.1:p.Thr372Ala
NR_045662.4:n.1773A>G
NR_045663.4:n.2449A>G
NM_001256267.2:c.2236A>G	NP_001243196.1:p.Thr746Ala
NM_001256268.2:c.1354A>G	NP_001243197.1:p.Thr452Ala
NM_032578.4:c.2236A>G MANE Select	NP_115967.2:p.Thr746Ala