Canonical Allele Identifier: CA2788367470

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195665_68195666insAATT , CM000672.2:g.68195665_68195666insAATT	GRCh38
NC_000010.10:g.69955422_69955423insAATT , CM000672.1:g.69955422_69955423insAATT	GRCh37
NC_000010.9:g.69625428_69625429insAATT	NCBI36
NG_032118.1:g.94549_94550insAATT , LRG_410:g.94549_94550insAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2333+133_2333+134insAATT	ENSP00000346369.2:n.2333+133_2333+134insAATT
ENST00000540630.6:c.3212+133_3212+134insAATT	ENSP00000441668.3:n.3212+133_3212+134insAATT
ENST00000613327.5:c.3158+133_3158+134insAATT	ENSP00000480757.2:n.3158+133_3158+134insAATT
ENST00000688812.1:c.*421+133_*421+134insAATT	ENSP00000510658.1:n.*421+133_*421+134insAATT
ENST00000690544.1:c.*2429+133_*2429+134insAATT	ENSP00000508989.1:n.*2429+133_*2429+134insAATT
ENST00000358913.10:c.3158+133_3158+134insAATT MANE Select	ENSP00000351790.5:n.3158+133_3158+134insAATT
ENST00000354393.6:c.2333+133_2333+134insAATT	ENSP00000346369.2:n.2333+133_2333+134insAATT
ENST00000358913.9:c.3158+133_3158+134insAATT	ENSP00000351790.5:n.3158+133_3158+134insAATT
ENST00000540630.5:c.3158+133_3158+134insAATT	ENSP00000441668.2:n.3158+133_3158+134insAATT
ENST00000613327.4:c.2276+133_2276+134insAATT	ENSP00000480757.1:n.2276+133_2276+134insAATT
NM_001256267.1:c.3158+133_3158+134insAATT	NP_001243196.1:n.3158+133_3158+134insAATT
NM_001256268.1:c.2276+133_2276+134insAATT	NP_001243197.1:n.2276+133_2276+134insAATT
NM_032578.3:c.3158+133_3158+134insAATT , LRG_410t1:c.3158+133_3158+134insAATT	NP_115967.2:n.3158+133_3158+134insAATT
NR_045662.3:n.2585+133_2585+134insAATT
NR_045663.3:n.3287+133_3287+134insAATT
XM_006718043.2:c.3212+133_3212+134insAATT	XP_006718106.1:n.3212+133_3212+134insAATT
XM_011540292.1:c.3188+133_3188+134insAATT	XP_011538594.1:n.3188+133_3188+134insAATT
XM_017016833.1:c.3236+133_3236+134insAATT	XP_016872322.1:n.3236+133_3236+134insAATT
XM_017016834.2:c.3158+133_3158+134insAATT	XP_016872323.1:n.3158+133_3158+134insAATT
XM_024448236.1:c.2036+133_2036+134insAATT	XP_024304004.1:n.2036+133_2036+134insAATT
NR_045662.4:n.2695+133_2695+134insAATT
NR_045663.4:n.3232+133_3232+134insAATT
NM_001256267.2:c.3158+133_3158+134insAATT	NP_001243196.1:n.3158+133_3158+134insAATT
NM_001256268.2:c.2276+133_2276+134insAATT	NP_001243197.1:n.2276+133_2276+134insAATT
NM_032578.4:c.3158+133_3158+134insAATT MANE Select	NP_115967.2:n.3158+133_3158+134insAATT