Canonical Allele Identifier: CA2574562542

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210557del , CM000672.2:g.68210557del	GRCh38
NC_000010.10:g.69970314del , CM000672.1:g.69970314del	GRCh37
NC_000010.9:g.69640320del	NCBI36
NG_032118.1:g.109441del , LRG_410:g.109441del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*102del	ENSP00000346369.2:n.*102del
ENST00000540630.6:c.*102del	ENSP00000441668.3:n.*102del
ENST00000613327.5:c.*102del	ENSP00000480757.2:n.*102del
ENST00000688812.1:c.*1328del	ENSP00000510658.1:n.*1328del
ENST00000690544.1:c.*3336del	ENSP00000508989.1:n.*3336del
ENST00000358913.10:c.*102del MANE Select	ENSP00000351790.5:n.*102del
ENST00000354393.6:c.*102del	ENSP00000346369.2:n.*102del
ENST00000358913.9:c.*102del	ENSP00000351790.5:n.*102del
ENST00000540630.5:c.*102del	ENSP00000441668.2:n.*102del
ENST00000613327.4:c.*102del	ENSP00000480757.1:n.*102del
NM_001256267.1:c.*102del	NP_001243196.1:n.*102del
NM_001256268.1:c.*102del	NP_001243197.1:n.*102del
NM_032578.3:c.*102del , LRG_410t1:c.*102del	NP_115967.2:n.*102del
NR_045662.3:n.3492del
NR_045663.3:n.4194del
XM_006718043.2:c.*102del	XP_006718106.1:n.*102del
XM_011540292.1:c.*102del	XP_011538594.1:n.*102del
XR_946029.1:n.1574+4733del
XM_017016833.1:c.*102del	XP_016872322.1:n.*102del
XM_017016834.2:c.*102del	XP_016872323.1:n.*102del
XM_024448236.1:c.*102del	XP_024304004.1:n.*102del
NR_045662.4:n.3602del
NR_045663.4:n.4139del
NM_001256267.2:c.*102del	NP_001243196.1:n.*102del
NM_001256268.2:c.*102del	NP_001243197.1:n.*102del
NM_032578.4:c.*102del MANE Select	NP_115967.2:n.*102del