Canonical Allele Identifier: CA2580081722

Gene: MYPN

Linked Data

• ClinVar Variation Id: 2112550
• ClinVar RCV Id: RCV003034623

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199491dup , CM000672.2:g.68199491dup	GRCh38
NC_000010.10:g.69959248dup , CM000672.1:g.69959248dup	GRCh37
NC_000010.9:g.69629254dup	NCBI36
NG_032118.1:g.98375dup , LRG_410:g.98375dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2584dup	ENSP00000346369.2:p.Thr862AsnfsTer9
ENST00000540630.6:c.3463dup	ENSP00000441668.3:p.Thr1155AsnfsTer9
ENST00000613327.5:c.3409dup	ENSP00000480757.2:p.Thr1137AsnfsTer9
ENST00000688812.1:c.*672dup	ENSP00000510658.1:n.*672dup
ENST00000690544.1:c.*2680dup	ENSP00000508989.1:n.*2680dup
ENST00000358913.10:c.3409dup MANE Select	ENSP00000351790.5:p.Thr1137AsnfsTer9
ENST00000354393.6:c.2584dup	ENSP00000346369.2:p.Thr862AsnfsTer9
ENST00000358913.9:c.3409dup	ENSP00000351790.5:p.Thr1137AsnfsTer9
ENST00000540630.5:c.3409dup	ENSP00000441668.2:p.Thr1137AsnfsTer9
ENST00000613327.4:c.2527dup	ENSP00000480757.1:p.Thr843AsnfsTer9
NM_001256267.1:c.3409dup	NP_001243196.1:p.Thr1137AsnfsTer9
NM_001256268.1:c.2527dup	NP_001243197.1:p.Thr843AsnfsTer9
NM_032578.3:c.3409dup , LRG_410t1:c.3409dup	NP_115967.2:p.Thr1137AsnfsTer9
NR_045662.3:n.2836dup
NR_045663.3:n.3538dup
XM_006718043.2:c.3463dup	XP_006718106.1:p.Thr1155AsnfsTer9
XM_011540292.1:c.3439dup	XP_011538594.1:p.Thr1147AsnfsTer9
XR_946029.1:n.1804-216dup
XM_017016833.1:c.3487dup	XP_016872322.1:p.Thr1163AsnfsTer9
XM_017016834.2:c.3409dup	XP_016872323.1:p.Thr1137AsnfsTer9
XM_024448236.1:c.2287dup	XP_024304004.1:p.Thr763AsnfsTer9
NR_045662.4:n.2946dup
NR_045663.4:n.3483dup
NM_001256267.2:c.3409dup	NP_001243196.1:p.Thr1137AsnfsTer9
NM_001256268.2:c.2527dup	NP_001243197.1:p.Thr843AsnfsTer9
NM_032578.4:c.3409dup MANE Select	NP_115967.2:p.Thr1137AsnfsTer9