Canonical Allele Identifier: CA376859249

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199484C>G , CM000672.2:g.68199484C>G	GRCh38
NC_000010.10:g.69959241C>G , CM000672.1:g.69959241C>G	GRCh37
NC_000010.9:g.69629247C>G	NCBI36
NG_032118.1:g.98368C>G , LRG_410:g.98368C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3402C>G MANE Select	NP_115967.2:p.Asp1134Glu
ENST00000358913.10:c.3402C>G MANE Select	ENSP00000351790.5:p.Asp1134Glu
NM_001256267.1:c.3402C>G	NP_001243196.1:p.Asp1134Glu
NM_001256267.2:c.3402C>G	NP_001243196.1:p.Asp1134Glu
NM_001256268.1:c.2520C>G	NP_001243197.1:p.Asp840Glu
NM_001256268.2:c.2520C>G	NP_001243197.1:p.Asp840Glu
NM_032578.3:c.3402C>G , LRG_410t1:c.3402C>G	NP_115967.2:p.Asp1134Glu
NR_045662.3:n.2829C>G
NR_045662.4:n.2939C>G
NR_045663.3:n.3531C>G
NR_045663.4:n.3476C>G
ENST00000354393.6:c.2577C>G	ENSP00000346369.2:p.Asp859Glu
ENST00000354393.7:c.2577C>G	ENSP00000346369.2:p.Asp859Glu
ENST00000358913.9:c.3402C>G	ENSP00000351790.5:p.Asp1134Glu
ENST00000540630.5:c.3402C>G	ENSP00000441668.2:p.Asp1134Glu
ENST00000540630.6:c.3456C>G	ENSP00000441668.3:p.Asp1152Glu
ENST00000613327.4:c.2520C>G	ENSP00000480757.1:p.Asp840Glu
ENST00000613327.5:c.3402C>G	ENSP00000480757.2:p.Asp1134Glu
ENST00000688812.1:c.*665C>G	ENSP00000510658.1:n.*665C>G
ENST00000690544.1:c.*2673C>G	ENSP00000508989.1:n.*2673C>G
XM_006718043.2:c.3456C>G	XP_006718106.1:p.Asp1152Glu
XM_011540292.1:c.3432C>G	XP_011538594.1:p.Asp1144Glu
XM_017016833.1:c.3480C>G	XP_016872322.1:p.Asp1160Glu
XM_017016834.2:c.3402C>G	XP_016872323.1:p.Asp1134Glu
XM_024448236.1:c.2280C>G	XP_024304004.1:p.Asp760Glu
XR_946029.1:n.1804-209G>C