Canonical Allele Identifier: CA335334

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68174320C>T , CM000672.2:g.68174320C>T	GRCh38
NC_000010.10:g.69934077C>T , CM000672.1:g.69934077C>T	GRCh37
NC_000010.9:g.69604083C>T	NCBI36
NG_032118.1:g.73204C>T , LRG_410:g.73204C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1403C>T	ENSP00000346369.2:p.Pro468Leu
ENST00000540630.6:c.2282C>T	ENSP00000441668.3:p.Pro761Leu
ENST00000613327.5:c.2228C>T	ENSP00000480757.2:p.Pro743Leu
ENST00000688812.1:c.2204C>T	ENSP00000510658.1:p.Pro735Leu
ENST00000690544.1:c.*1499C>T	ENSP00000508989.1:n.*1499C>T
ENST00000358913.10:c.2228C>T MANE Select	ENSP00000351790.5:p.Pro743Leu
ENST00000354393.6:c.1403C>T	ENSP00000346369.2:p.Pro468Leu
ENST00000358913.9:c.2228C>T	ENSP00000351790.5:p.Pro743Leu
ENST00000540630.5:c.2228C>T	ENSP00000441668.2:p.Pro743Leu
ENST00000613327.4:c.1346C>T	ENSP00000480757.1:p.Pro449Leu
NM_001256267.1:c.2228C>T	NP_001243196.1:p.Pro743Leu
NM_001256268.1:c.1346C>T	NP_001243197.1:p.Pro449Leu
NM_032578.3:c.2228C>T , LRG_410t1:c.2228C>T	NP_115967.2:p.Pro743Leu
NR_045662.3:n.1655C>T
NR_045663.3:n.2496C>T
XM_006718043.2:c.2282C>T	XP_006718106.1:p.Pro761Leu
XM_011540292.1:c.2258C>T	XP_011538594.1:p.Pro753Leu
XM_017016833.1:c.2306C>T	XP_016872322.1:p.Pro769Leu
XM_017016834.2:c.2228C>T	XP_016872323.1:p.Pro743Leu
XM_024448236.1:c.1106C>T	XP_024304004.1:p.Pro369Leu
NR_045662.4:n.1765C>T
NR_045663.4:n.2441C>T
NM_001256267.2:c.2228C>T	NP_001243196.1:p.Pro743Leu
NM_001256268.2:c.1346C>T	NP_001243197.1:p.Pro449Leu
NM_032578.4:c.2228C>T MANE Select	NP_115967.2:p.Pro743Leu