Canonical Allele Identifier: CA918698073

Gene: MYPN

Linked Data

• dbSNP Id: rs1564675417

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166628del , CM000672.2:g.68166628del	GRCh38
NC_000010.10:g.69926385del , CM000672.1:g.69926385del	GRCh37
NC_000010.9:g.69596391del	NCBI36
NG_032118.1:g.65512del , LRG_410:g.65512del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1110del	ENSP00000346369.2:p.Val371Ter
ENST00000373675.4:c.1935del	ENSP00000362779.4:p.Val646Ter
ENST00000540630.6:c.1989del	ENSP00000441668.3:p.Val664Ter
ENST00000613327.5:c.1935del	ENSP00000480757.2:p.Val646Ter
ENST00000687572.1:c.813del	ENSP00000510427.1:p.Val272Ter
ENST00000688812.1:c.1911del	ENSP00000510658.1:p.Val638Ter
ENST00000690544.1:c.*1206del	ENSP00000508989.1:n.*1206del
ENST00000358913.10:c.1935del MANE Select	ENSP00000351790.5:p.Val646Ter
ENST00000354393.6:c.1110del	ENSP00000346369.2:p.Val371Ter
ENST00000358913.9:c.1935del	ENSP00000351790.5:p.Val646Ter
ENST00000540630.5:c.1935del	ENSP00000441668.2:p.Val646Ter
ENST00000613327.4:c.1053del	ENSP00000480757.1:p.Val352Ter
NM_001256267.1:c.1935del	NP_001243196.1:p.Val646Ter
NM_001256268.1:c.1053del	NP_001243197.1:p.Val352Ter
NM_032578.3:c.1935del , LRG_410t1:c.1935del	NP_115967.2:p.Val646Ter
NR_045662.3:n.1362del
NR_045663.3:n.2203del
XM_006718043.2:c.1989del	XP_006718106.1:p.Val664Ter
XM_011540292.1:c.1965del	XP_011538594.1:p.Val656Ter
XM_017016833.1:c.2013del	XP_016872322.1:p.Val672Ter
XM_017016834.2:c.1935del	XP_016872323.1:p.Val646Ter
XM_024448236.1:c.813del	XP_024304004.1:p.Val272Ter
NR_045662.4:n.1472del
NR_045663.4:n.2148del
NM_001256267.2:c.1935del	NP_001243196.1:p.Val646Ter
NM_001256268.2:c.1053del	NP_001243197.1:p.Val352Ter
NM_032578.4:c.1935del MANE Select	NP_115967.2:p.Val646Ter