Canonical Allele Identifier: CA2609373569

Gene: MYPN

Linked Data

• gnomAD v4: 10-68199473-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199474del , CM000672.2:g.68199474del	GRCh38
NC_000010.10:g.69959231del , CM000672.1:g.69959231del	GRCh37
NC_000010.9:g.69629237del	NCBI36
NG_032118.1:g.98358del , LRG_410:g.98358del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2567del	ENSP00000346369.2:p.Leu856ArgfsTer?
ENST00000540630.6:c.3446del	ENSP00000441668.3:p.Leu1149ArgfsTer?
ENST00000613327.5:c.3392del	ENSP00000480757.2:p.Leu1131ArgfsTer?
ENST00000688812.1:c.*655del	ENSP00000510658.1:n.*655del
ENST00000690544.1:c.*2663del	ENSP00000508989.1:n.*2663del
ENST00000358913.10:c.3392del MANE Select	ENSP00000351790.5:p.Leu1131ArgfsTer?
ENST00000354393.6:c.2567del	ENSP00000346369.2:p.Leu856ArgfsTer?
ENST00000358913.9:c.3392del	ENSP00000351790.5:p.Leu1131ArgfsTer?
ENST00000540630.5:c.3392del	ENSP00000441668.2:p.Leu1131ArgfsTer?
ENST00000613327.4:c.2510del	ENSP00000480757.1:p.Leu837ArgfsTer?
NM_001256267.1:c.3392del	NP_001243196.1:p.Leu1131ArgfsTer?
NM_001256268.1:c.2510del	NP_001243197.1:p.Leu837ArgfsTer?
NM_032578.3:c.3392del , LRG_410t1:c.3392del	NP_115967.2:p.Leu1131ArgfsTer?
NR_045662.3:n.2819del
NR_045663.3:n.3521del
XM_006718043.2:c.3446del	XP_006718106.1:p.Leu1149ArgfsTer?
XM_011540292.1:c.3422del	XP_011538594.1:p.Leu1141ArgfsTer?
XR_946029.1:n.1804-199del
XM_017016833.1:c.3470del	XP_016872322.1:p.Leu1157ArgfsTer?
XM_017016834.2:c.3392del	XP_016872323.1:p.Leu1131ArgfsTer?
XM_024448236.1:c.2270del	XP_024304004.1:p.Leu757ArgfsTer?
NR_045662.4:n.2929del
NR_045663.4:n.3466del
NM_001256267.2:c.3392del	NP_001243196.1:p.Leu1131ArgfsTer?
NM_001256268.2:c.2510del	NP_001243197.1:p.Leu837ArgfsTer?
NM_032578.4:c.3392del MANE Select	NP_115967.2:p.Leu1131ArgfsTer?