Canonical Allele Identifier: CA376859321

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199519G>A , CM000672.2:g.68199519G>A	GRCh38
NC_000010.10:g.69959276G>A , CM000672.1:g.69959276G>A	GRCh37
NC_000010.9:g.69629282G>A	NCBI36
NG_032118.1:g.98403G>A , LRG_410:g.98403G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3437G>A MANE Select	NP_115967.2:p.Cys1146Tyr
ENST00000358913.10:c.3437G>A MANE Select	ENSP00000351790.5:p.Cys1146Tyr
NM_001256267.1:c.3437G>A	NP_001243196.1:p.Cys1146Tyr
NM_001256267.2:c.3437G>A	NP_001243196.1:p.Cys1146Tyr
NM_001256268.1:c.2555G>A	NP_001243197.1:p.Cys852Tyr
NM_001256268.2:c.2555G>A	NP_001243197.1:p.Cys852Tyr
NM_032578.3:c.3437G>A , LRG_410t1:c.3437G>A	NP_115967.2:p.Cys1146Tyr
NR_045662.3:n.2864G>A
NR_045662.4:n.2974G>A
NR_045663.3:n.3566G>A
NR_045663.4:n.3511G>A
ENST00000354393.6:c.2612G>A	ENSP00000346369.2:p.Cys871Tyr
ENST00000354393.7:c.2612G>A	ENSP00000346369.2:p.Cys871Tyr
ENST00000358913.9:c.3437G>A	ENSP00000351790.5:p.Cys1146Tyr
ENST00000540630.5:c.3437G>A	ENSP00000441668.2:p.Cys1146Tyr
ENST00000540630.6:c.3491G>A	ENSP00000441668.3:p.Cys1164Tyr
ENST00000613327.4:c.2555G>A	ENSP00000480757.1:p.Cys852Tyr
ENST00000613327.5:c.3437G>A	ENSP00000480757.2:p.Cys1146Tyr
ENST00000688812.1:c.*700G>A	ENSP00000510658.1:n.*700G>A
ENST00000690544.1:c.*2708G>A	ENSP00000508989.1:n.*2708G>A
XM_006718043.2:c.3491G>A	XP_006718106.1:p.Cys1164Tyr
XM_011540292.1:c.3467G>A	XP_011538594.1:p.Cys1156Tyr
XM_017016833.1:c.3515G>A	XP_016872322.1:p.Cys1172Tyr
XM_017016834.2:c.3437G>A	XP_016872323.1:p.Cys1146Tyr
XM_024448236.1:c.2315G>A	XP_024304004.1:p.Cys772Tyr
XR_946029.1:n.1804-244C>T