Canonical Allele Identifier: CA593850902

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199514del , CM000672.2:g.68199514del	GRCh38
NC_000010.10:g.69959271del , CM000672.1:g.69959271del	GRCh37
NC_000010.9:g.69629277del	NCBI36
NG_032118.1:g.98398del , LRG_410:g.98398del

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3432del MANE Select	NP_115967.2:p.Tyr1144Ter
ENST00000358913.10:c.3432del MANE Select	ENSP00000351790.5:p.Tyr1144Ter
NM_001256267.1:c.3432del	NP_001243196.1:p.Tyr1144Ter
NM_001256267.2:c.3432del	NP_001243196.1:p.Tyr1144Ter
NM_001256268.1:c.2550del	NP_001243197.1:p.Tyr850Ter
NM_001256268.2:c.2550del	NP_001243197.1:p.Tyr850Ter
NM_032578.3:c.3432del , LRG_410t1:c.3432del	NP_115967.2:p.Tyr1144Ter
NR_045662.3:n.2859del
NR_045662.4:n.2969del
NR_045663.3:n.3561del
NR_045663.4:n.3506del
ENST00000354393.6:c.2607del	ENSP00000346369.2:p.Tyr869Ter
ENST00000354393.7:c.2607del	ENSP00000346369.2:p.Tyr869Ter
ENST00000358913.9:c.3432del	ENSP00000351790.5:p.Tyr1144Ter
ENST00000540630.5:c.3432del	ENSP00000441668.2:p.Tyr1144Ter
ENST00000540630.6:c.3486del	ENSP00000441668.3:p.Tyr1162Ter
ENST00000613327.4:c.2550del	ENSP00000480757.1:p.Tyr850Ter
ENST00000613327.5:c.3432del	ENSP00000480757.2:p.Tyr1144Ter
ENST00000688812.1:c.*695del	ENSP00000510658.1:n.*695del
ENST00000690544.1:c.*2703del	ENSP00000508989.1:n.*2703del
XM_006718043.2:c.3486del	XP_006718106.1:p.Tyr1162Ter
XM_011540292.1:c.3462del	XP_011538594.1:p.Tyr1154Ter
XM_017016833.1:c.3510del	XP_016872322.1:p.Tyr1170Ter
XM_017016834.2:c.3432del	XP_016872323.1:p.Tyr1144Ter
XM_024448236.1:c.2310del	XP_024304004.1:p.Tyr770Ter
XR_946029.1:n.1804-239del