Canonical Allele Identifier: CA2609373566

Gene: MYPN

Linked Data

• gnomAD v4: 10-68199382-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199387del , CM000672.2:g.68199387del	GRCh38
NC_000010.10:g.69959144del , CM000672.1:g.69959144del	GRCh37
NC_000010.9:g.69629150del	NCBI36
NG_032118.1:g.98271del , LRG_410:g.98271del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2480del	ENSP00000346369.2:p.Pro827ArgfsTer3
ENST00000540630.6:c.3359del	ENSP00000441668.3:p.Pro1120ArgfsTer3
ENST00000613327.5:c.3305del	ENSP00000480757.2:p.Pro1102ArgfsTer3
ENST00000688812.1:c.*568del	ENSP00000510658.1:n.*568del
ENST00000690544.1:c.*2576del	ENSP00000508989.1:n.*2576del
ENST00000358913.10:c.3305del MANE Select	ENSP00000351790.5:p.Pro1102ArgfsTer3
ENST00000354393.6:c.2480del	ENSP00000346369.2:p.Pro827ArgfsTer3
ENST00000358913.9:c.3305del	ENSP00000351790.5:p.Pro1102ArgfsTer3
ENST00000540630.5:c.3305del	ENSP00000441668.2:p.Pro1102ArgfsTer3
ENST00000613327.4:c.2423del	ENSP00000480757.1:p.Pro808ArgfsTer3
NM_001256267.1:c.3305del	NP_001243196.1:p.Pro1102ArgfsTer3
NM_001256268.1:c.2423del	NP_001243197.1:p.Pro808ArgfsTer3
NM_032578.3:c.3305del , LRG_410t1:c.3305del	NP_115967.2:p.Pro1102ArgfsTer3
NR_045662.3:n.2732del
NR_045663.3:n.3434del
XM_006718043.2:c.3359del	XP_006718106.1:p.Pro1120ArgfsTer3
XM_011540292.1:c.3335del	XP_011538594.1:p.Pro1112ArgfsTer3
XR_946029.1:n.1804-108del
XM_017016833.1:c.3383del	XP_016872322.1:p.Pro1128ArgfsTer3
XM_017016834.2:c.3305del	XP_016872323.1:p.Pro1102ArgfsTer3
XM_024448236.1:c.2183del	XP_024304004.1:p.Pro728ArgfsTer3
NR_045662.4:n.2842del
NR_045663.4:n.3379del
NM_001256267.2:c.3305del	NP_001243196.1:p.Pro1102ArgfsTer3
NM_001256268.2:c.2423del	NP_001243197.1:p.Pro808ArgfsTer3
NM_032578.4:c.3305del MANE Select	NP_115967.2:p.Pro1102ArgfsTer3