Canonical Allele Identifier: CA653371635

Gene: MYPN

Linked Data

• COSMIC: COSN22699173

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210524dup , CM000672.2:g.68210524dup	GRCh38
NC_000010.10:g.69970281dup , CM000672.1:g.69970281dup	GRCh37
NC_000010.9:g.69640287dup	NCBI36
NG_032118.1:g.109408dup , LRG_410:g.109408dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*69dup	ENSP00000346369.2:n.*69dup
ENST00000540630.6:c.*69dup	ENSP00000441668.3:n.*69dup
ENST00000613327.5:c.*69dup	ENSP00000480757.2:n.*69dup
ENST00000688812.1:c.*1295dup	ENSP00000510658.1:n.*1295dup
ENST00000690544.1:c.*3303dup	ENSP00000508989.1:n.*3303dup
ENST00000358913.10:c.*69dup MANE Select	ENSP00000351790.5:n.*69dup
ENST00000354393.6:c.*69dup	ENSP00000346369.2:n.*69dup
ENST00000358913.9:c.*69dup	ENSP00000351790.5:n.*69dup
ENST00000540630.5:c.*69dup	ENSP00000441668.2:n.*69dup
ENST00000613327.4:c.*69dup	ENSP00000480757.1:n.*69dup
NM_001256267.1:c.*69dup	NP_001243196.1:n.*69dup
NM_001256268.1:c.*69dup	NP_001243197.1:n.*69dup
NM_032578.3:c.*69dup , LRG_410t1:c.*69dup	NP_115967.2:n.*69dup
NR_045662.3:n.3459dup
NR_045663.3:n.4161dup
XM_006718043.2:c.*69dup	XP_006718106.1:n.*69dup
XM_011540292.1:c.*69dup	XP_011538594.1:n.*69dup
XR_946029.1:n.1574+4764dup
XM_017016833.1:c.*69dup	XP_016872322.1:n.*69dup
XM_017016834.2:c.*69dup	XP_016872323.1:n.*69dup
XM_024448236.1:c.*69dup	XP_024304004.1:n.*69dup
NR_045662.4:n.3569dup
NR_045663.4:n.4106dup
NM_001256267.2:c.*69dup	NP_001243196.1:n.*69dup
NM_001256268.2:c.*69dup	NP_001243197.1:n.*69dup
NM_032578.4:c.*69dup MANE Select	NP_115967.2:n.*69dup