Canonical Allele Identifier: CA1917225578

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195500_68195501delinsCA , CM000672.2:g.68195500_68195501delinsCA	GRCh38
NC_000010.10:g.69955257_69955258delinsCA , CM000672.1:g.69955257_69955258delinsCA	GRCh37
NC_000010.9:g.69625263_69625264delinsCA	NCBI36
NG_032118.1:g.94384_94385delinsCA , LRG_410:g.94384_94385delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2301_2302delinsCA	ENSP00000346369.2:p.Arg767=
ENST00000540630.6:c.3180_3181delinsCA	ENSP00000441668.3:p.Arg1060=
ENST00000613327.5:c.3126_3127delinsCA	ENSP00000480757.2:p.Arg1042=
ENST00000688812.1:c.*389_*390delinsCA	ENSP00000510658.1:n.*389_*390delinsCA
ENST00000690544.1:c.*2397_*2398delinsCA	ENSP00000508989.1:n.*2397_*2398delinsCA
ENST00000358913.10:c.3126_3127delinsCA MANE Select	ENSP00000351790.5:p.Arg1042=
ENST00000354393.6:c.2301_2302delinsCA	ENSP00000346369.2:p.Arg767=
ENST00000358913.9:c.3126_3127delinsCA	ENSP00000351790.5:p.Arg1042=
ENST00000540630.5:c.3126_3127delinsCA	ENSP00000441668.2:p.Arg1042=
ENST00000613327.4:c.2244_2245delinsCA	ENSP00000480757.1:p.Arg748=
NM_001256267.1:c.3126_3127delinsCA	NP_001243196.1:p.Arg1042=
NM_001256268.1:c.2244_2245delinsCA	NP_001243197.1:p.Arg748=
NM_032578.3:c.3126_3127delinsCA , LRG_410t1:c.3126_3127delinsCA	NP_115967.2:p.Arg1042=
NR_045662.3:n.2553_2554delinsCA
NR_045663.3:n.3255_3256delinsCA
XM_006718043.2:c.3180_3181delinsCA	XP_006718106.1:p.Arg1060=
XM_011540292.1:c.3156_3157delinsCA	XP_011538594.1:p.Arg1052=
XM_017016833.1:c.3204_3205delinsCA	XP_016872322.1:p.Arg1068=
XM_017016834.2:c.3126_3127delinsCA	XP_016872323.1:p.Arg1042=
XM_024448236.1:c.2004_2005delinsCA	XP_024304004.1:p.Arg668=
NR_045662.4:n.2663_2664delinsCA
NR_045663.4:n.3200_3201delinsCA
NM_001256267.2:c.3126_3127delinsCA	NP_001243196.1:p.Arg1042=
NM_001256268.2:c.2244_2245delinsCA	NP_001243197.1:p.Arg748=
NM_032578.4:c.3126_3127delinsCA MANE Select	NP_115967.2:p.Arg1042=