Canonical Allele Identifier: CA469812478

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199511C>A , CM000672.2:g.68199511C>A	GRCh38
NC_000010.10:g.69959268C>A , CM000672.1:g.69959268C>A	GRCh37
NC_000010.9:g.69629274C>A	NCBI36
NG_032118.1:g.98395C>A , LRG_410:g.98395C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3429C>A MANE Select	NP_115967.2:p.Thr1143=
ENST00000358913.10:c.3429C>A MANE Select	ENSP00000351790.5:p.Thr1143=
NM_001256267.1:c.3429C>A	NP_001243196.1:p.Thr1143=
NM_001256267.2:c.3429C>A	NP_001243196.1:p.Thr1143=
NM_001256268.1:c.2547C>A	NP_001243197.1:p.Thr849=
NM_001256268.2:c.2547C>A	NP_001243197.1:p.Thr849=
NM_032578.3:c.3429C>A , LRG_410t1:c.3429C>A	NP_115967.2:p.Thr1143=
NR_045662.3:n.2856C>A
NR_045662.4:n.2966C>A
NR_045663.3:n.3558C>A
NR_045663.4:n.3503C>A
ENST00000354393.6:c.2604C>A	ENSP00000346369.2:p.Thr868=
ENST00000354393.7:c.2604C>A	ENSP00000346369.2:p.Thr868=
ENST00000358913.9:c.3429C>A	ENSP00000351790.5:p.Thr1143=
ENST00000540630.5:c.3429C>A	ENSP00000441668.2:p.Thr1143=
ENST00000540630.6:c.3483C>A	ENSP00000441668.3:p.Thr1161=
ENST00000613327.4:c.2547C>A	ENSP00000480757.1:p.Thr849=
ENST00000613327.5:c.3429C>A	ENSP00000480757.2:p.Thr1143=
ENST00000688812.1:c.*692C>A	ENSP00000510658.1:n.*692C>A
ENST00000690544.1:c.*2700C>A	ENSP00000508989.1:n.*2700C>A
XM_006718043.2:c.3483C>A	XP_006718106.1:p.Thr1161=
XM_011540292.1:c.3459C>A	XP_011538594.1:p.Thr1153=
XM_017016833.1:c.3507C>A	XP_016872322.1:p.Thr1169=
XM_017016834.2:c.3429C>A	XP_016872323.1:p.Thr1143=
XM_024448236.1:c.2307C>A	XP_024304004.1:p.Thr769=
XR_946029.1:n.1804-236G>T