Canonical Allele Identifier: CA1917192601

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68122194_68122195delinsAG , CM000672.2:g.68122194_68122195delinsAG	GRCh38
NC_000010.10:g.69881951_69881952delinsAG , CM000672.1:g.69881951_69881952delinsAG	GRCh37
NC_000010.9:g.69551957_69551958delinsAG	NCBI36
NG_032118.1:g.21078_21079delinsAG , LRG_410:g.21078_21079delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.77+15393_77+15394delinsAG	ENSP00000346369.2:n.77+15393_77+15394delinsAG
ENST00000373675.4:c.756_757delinsAG	ENSP00000362779.4:p.Pro252=
ENST00000540630.6:c.756_757delinsAG	ENSP00000441668.3:p.Pro252=
ENST00000613327.5:c.756_757delinsAG	ENSP00000480757.2:p.Pro252=
ENST00000685006.1:c.828_829delinsAG	ENSP00000510318.1:p.Pro276=
ENST00000685060.1:n.993_994delinsAG
ENST00000685154.1:c.756_757delinsAG	ENSP00000509251.1:p.Pro252=
ENST00000685627.1:c.*767_*768delinsAG	ENSP00000508637.1:n.*767_*768delinsAG
ENST00000686289.1:n.113+16011_113+16012delinsAG
ENST00000687572.1:c.-221+16011_-221+16012delinsAG	ENSP00000510427.1:n.-221+16011_-221+16012delinsAG
ENST00000687705.1:c.*1005_*1006delinsAG	ENSP00000509639.1:n.*1005_*1006delinsAG
ENST00000688812.1:c.756_757delinsAG	ENSP00000510658.1:p.Pro252=
ENST00000689218.1:n.985_986delinsAG
ENST00000689484.1:c.-220-20746_-220-20745delinsAG	ENSP00000509884.1:n.-220-20746_-220-20745delinsAG
ENST00000689797.1:c.-220-20746_-220-20745delinsAG	ENSP00000510689.1:n.-220-20746_-220-20745delinsAG
ENST00000690544.1:c.756_757delinsAG	ENSP00000508989.1:p.Pro252=
ENST00000692038.1:c.*1005_*1006delinsAG	ENSP00000509220.1:n.*1005_*1006delinsAG
ENST00000692953.1:n.62+16011_62+16012delinsAG
ENST00000692979.1:c.756_757delinsAG	ENSP00000509849.1:p.Pro252=
ENST00000358913.10:c.756_757delinsAG MANE Select	ENSP00000351790.5:p.Pro252=
ENST00000354393.6:c.77+15393_77+15394delinsAG	ENSP00000346369.2:n.77+15393_77+15394delinsAG
ENST00000358913.9:c.756_757delinsAG	ENSP00000351790.5:p.Pro252=
ENST00000373675.3:c.756_757delinsAG	ENSP00000362779.3:p.Pro252=
ENST00000540630.5:c.756_757delinsAG	ENSP00000441668.2:p.Pro252=
ENST00000613327.4:c.-367_-366delinsAG	ENSP00000480757.1:n.-367_-366delinsAG
NM_001256267.1:c.756_757delinsAG	NP_001243196.1:p.Pro252=
NM_001256268.1:c.-367_-366delinsAG	NP_001243197.1:n.-367_-366delinsAG
NM_032578.3:c.756_757delinsAG , LRG_410t1:c.756_757delinsAG	NP_115967.2:p.Pro252=
NR_045662.3:n.329+15393_329+15394delinsAG
NR_045663.3:n.1048_1049delinsAG
XM_006718043.2:c.756_757delinsAG	XP_006718106.1:p.Pro252=
XM_011540292.1:c.756_757delinsAG	XP_011538594.1:p.Pro252=
XM_017016833.1:c.834_835delinsAG	XP_016872322.1:p.Pro278=
XM_017016834.2:c.756_757delinsAG	XP_016872323.1:p.Pro252=
XM_024448236.1:c.-221+16011_-221+16012delinsAG	XP_024304004.1:n.-221+16011_-221+16012delinsAG
NR_045662.4:n.439+15393_439+15394delinsAG
NR_045663.4:n.993_994delinsAG
NM_001256267.2:c.756_757delinsAG	NP_001243196.1:p.Pro252=
NM_001256268.2:c.-367_-366delinsAG	NP_001243197.1:n.-367_-366delinsAG
NM_032578.4:c.756_757delinsAG MANE Select	NP_115967.2:p.Pro252=