Canonical Allele Identifier: CA376858995

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199410G>T , CM000672.2:g.68199410G>T	GRCh38
NC_000010.10:g.69959167G>T , CM000672.1:g.69959167G>T	GRCh37
NC_000010.9:g.69629173G>T	NCBI36
NG_032118.1:g.98294G>T , LRG_410:g.98294G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3328G>T MANE Select	NP_115967.2:p.Gly1110Cys
ENST00000358913.10:c.3328G>T MANE Select	ENSP00000351790.5:p.Gly1110Cys
NM_001256267.1:c.3328G>T	NP_001243196.1:p.Gly1110Cys
NM_001256267.2:c.3328G>T	NP_001243196.1:p.Gly1110Cys
NM_001256268.1:c.2446G>T	NP_001243197.1:p.Gly816Cys
NM_001256268.2:c.2446G>T	NP_001243197.1:p.Gly816Cys
NM_032578.3:c.3328G>T , LRG_410t1:c.3328G>T	NP_115967.2:p.Gly1110Cys
NR_045662.3:n.2755G>T
NR_045662.4:n.2865G>T
NR_045663.3:n.3457G>T
NR_045663.4:n.3402G>T
ENST00000354393.6:c.2503G>T	ENSP00000346369.2:p.Gly835Cys
ENST00000354393.7:c.2503G>T	ENSP00000346369.2:p.Gly835Cys
ENST00000358913.9:c.3328G>T	ENSP00000351790.5:p.Gly1110Cys
ENST00000540630.5:c.3328G>T	ENSP00000441668.2:p.Gly1110Cys
ENST00000540630.6:c.3382G>T	ENSP00000441668.3:p.Gly1128Cys
ENST00000613327.4:c.2446G>T	ENSP00000480757.1:p.Gly816Cys
ENST00000613327.5:c.3328G>T	ENSP00000480757.2:p.Gly1110Cys
ENST00000688812.1:c.*591G>T	ENSP00000510658.1:n.*591G>T
ENST00000690544.1:c.*2599G>T	ENSP00000508989.1:n.*2599G>T
XM_006718043.2:c.3382G>T	XP_006718106.1:p.Gly1128Cys
XM_011540292.1:c.3358G>T	XP_011538594.1:p.Gly1120Cys
XM_017016833.1:c.3406G>T	XP_016872322.1:p.Gly1136Cys
XM_017016834.2:c.3328G>T	XP_016872323.1:p.Gly1110Cys
XM_024448236.1:c.2206G>T	XP_024304004.1:p.Gly736Cys
XR_946029.1:n.1804-135C>A