Canonical Allele Identifier: CA1917192644

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68122280_68122283delinsCAGA , CM000672.2:g.68122280_68122283delinsCAGA	GRCh38
NC_000010.10:g.69882037_69882040delinsCAGA , CM000672.1:g.69882037_69882040delinsCAGA	GRCh37
NC_000010.9:g.69552043_69552046delinsCAGA	NCBI36
NG_032118.1:g.21164_21167delinsCAGA , LRG_410:g.21164_21167delinsCAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.77+15479_77+15482delinsCAGA	ENSP00000346369.2:n.77+15479_77+15482delinsCAGA
ENST00000373675.4:c.842_845delinsCAGA	ENSP00000362779.4:p.Pro281=
ENST00000540630.6:c.842_845delinsCAGA	ENSP00000441668.3:p.Pro281=
ENST00000613327.5:c.842_845delinsCAGA	ENSP00000480757.2:p.Pro281=
ENST00000685006.1:c.914_917delinsCAGA	ENSP00000510318.1:p.Pro305=
ENST00000685060.1:n.1079_1082delinsCAGA
ENST00000685154.1:c.842_845delinsCAGA	ENSP00000509251.1:p.Pro281=
ENST00000685627.1:c.*853_*856delinsCAGA	ENSP00000508637.1:n.*853_*856delinsCAGA
ENST00000686289.1:n.113+16097_113+16100delinsCAGA
ENST00000687572.1:c.-221+16097_-221+16100delinsCAGA	ENSP00000510427.1:n.-221+16097_-221+16100delinsCAGA
ENST00000687705.1:c.*1091_*1094delinsCAGA	ENSP00000509639.1:n.*1091_*1094delinsCAGA
ENST00000688812.1:c.842_845delinsCAGA	ENSP00000510658.1:p.Pro281=
ENST00000689218.1:n.1071_1074delinsCAGA
ENST00000689484.1:c.-220-20660_-220-20657delinsCAGA	ENSP00000509884.1:n.-220-20660_-220-20657delinsCAGA
ENST00000689797.1:c.-220-20660_-220-20657delinsCAGA	ENSP00000510689.1:n.-220-20660_-220-20657delinsCAGA
ENST00000690544.1:c.842_845delinsCAGA	ENSP00000508989.1:p.Pro281=
ENST00000692038.1:c.*1091_*1094delinsCAGA	ENSP00000509220.1:n.*1091_*1094delinsCAGA
ENST00000692953.1:n.62+16097_62+16100delinsCAGA
ENST00000692979.1:c.842_845delinsCAGA	ENSP00000509849.1:p.Pro281=
ENST00000358913.10:c.842_845delinsCAGA MANE Select	ENSP00000351790.5:p.Pro281=
ENST00000354393.6:c.77+15479_77+15482delinsCAGA	ENSP00000346369.2:n.77+15479_77+15482delinsCAGA
ENST00000358913.9:c.842_845delinsCAGA	ENSP00000351790.5:p.Pro281=
ENST00000373675.3:c.842_845delinsCAGA	ENSP00000362779.3:p.Pro281=
ENST00000540630.5:c.842_845delinsCAGA	ENSP00000441668.2:p.Pro281=
ENST00000613327.4:c.-281_-278delinsCAGA	ENSP00000480757.1:n.-281_-278delinsCAGA
NM_001256267.1:c.842_845delinsCAGA	NP_001243196.1:p.Pro281=
NM_001256268.1:c.-281_-278delinsCAGA	NP_001243197.1:n.-281_-278delinsCAGA
NM_032578.3:c.842_845delinsCAGA , LRG_410t1:c.842_845delinsCAGA	NP_115967.2:p.Pro281=
NR_045662.3:n.329+15479_329+15482delinsCAGA
NR_045663.3:n.1134_1137delinsCAGA
XM_006718043.2:c.842_845delinsCAGA	XP_006718106.1:p.Pro281=
XM_011540292.1:c.842_845delinsCAGA	XP_011538594.1:p.Pro281=
XM_017016833.1:c.920_923delinsCAGA	XP_016872322.1:p.Pro307=
XM_017016834.2:c.842_845delinsCAGA	XP_016872323.1:p.Pro281=
XM_024448236.1:c.-221+16097_-221+16100delinsCAGA	XP_024304004.1:n.-221+16097_-221+16100delinsCAGA
NR_045662.4:n.439+15479_439+15482delinsCAGA
NR_045663.4:n.1079_1082delinsCAGA
NM_001256267.2:c.842_845delinsCAGA	NP_001243196.1:p.Pro281=
NM_001256268.2:c.-281_-278delinsCAGA	NP_001243197.1:n.-281_-278delinsCAGA
NM_032578.4:c.842_845delinsCAGA MANE Select	NP_115967.2:p.Pro281=