Canonical Allele Identifier: CA2609374247

Gene: MYPN

Linked Data

• gnomAD v4: 10-68210573-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210573_68210574insA , CM000672.2:g.68210573_68210574insA	GRCh38
NC_000010.10:g.69970330_69970331insA , CM000672.1:g.69970330_69970331insA	GRCh37
NC_000010.9:g.69640336_69640337insA	NCBI36
NG_032118.1:g.109457_109458insA , LRG_410:g.109457_109458insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*118_*119insA	ENSP00000346369.2:n.*118_*119insA
ENST00000540630.6:c.*118_*119insA	ENSP00000441668.3:n.*118_*119insA
ENST00000613327.5:c.*118_*119insA	ENSP00000480757.2:n.*118_*119insA
ENST00000688812.1:c.*1344_*1345insA	ENSP00000510658.1:n.*1344_*1345insA
ENST00000690544.1:c.*3352_*3353insA	ENSP00000508989.1:n.*3352_*3353insA
ENST00000358913.10:c.*118_*119insA MANE Select	ENSP00000351790.5:n.*118_*119insA
ENST00000354393.6:c.*118_*119insA	ENSP00000346369.2:n.*118_*119insA
ENST00000358913.9:c.*118_*119insA	ENSP00000351790.5:n.*118_*119insA
ENST00000540630.5:c.*118_*119insA	ENSP00000441668.2:n.*118_*119insA
ENST00000613327.4:c.*118_*119insA	ENSP00000480757.1:n.*118_*119insA
NM_001256267.1:c.*118_*119insA	NP_001243196.1:n.*118_*119insA
NM_001256268.1:c.*118_*119insA	NP_001243197.1:n.*118_*119insA
NM_032578.3:c.*118_*119insA , LRG_410t1:c.*118_*119insA	NP_115967.2:n.*118_*119insA
NR_045662.3:n.3508_3509insA
NR_045663.3:n.4210_4211insA
XM_006718043.2:c.*118_*119insA	XP_006718106.1:n.*118_*119insA
XM_011540292.1:c.*118_*119insA	XP_011538594.1:n.*118_*119insA
XR_946029.1:n.1574+4714_1574+4715insT
XM_017016833.1:c.*118_*119insA	XP_016872322.1:n.*118_*119insA
XM_017016834.2:c.*118_*119insA	XP_016872323.1:n.*118_*119insA
XM_024448236.1:c.*118_*119insA	XP_024304004.1:n.*118_*119insA
NR_045662.4:n.3618_3619insA
NR_045663.4:n.4155_4156insA
NM_001256267.2:c.*118_*119insA	NP_001243196.1:n.*118_*119insA
NM_001256268.2:c.*118_*119insA	NP_001243197.1:n.*118_*119insA
NM_032578.4:c.*118_*119insA MANE Select	NP_115967.2:n.*118_*119insA