Canonical Allele Identifier: CA376858173

Gene: MYPN

Linked Data

• COSMIC: COSM919667
• MyVariant Identifiers: chr10:g.69957130A>C (hg19) ; chr10:g.68197373A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68197373A>C , CM000672.2:g.68197373A>C	GRCh38
NC_000010.10:g.69957130A>C , CM000672.1:g.69957130A>C	GRCh37
NC_000010.9:g.69627136A>C	NCBI36
NG_032118.1:g.96257A>C , LRG_410:g.96257A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2355A>C	ENSP00000346369.2:p.Glu785Asp
ENST00000540630.6:c.3234A>C	ENSP00000441668.3:p.Glu1078Asp
ENST00000613327.5:c.3180A>C	ENSP00000480757.2:p.Glu1060Asp
ENST00000688812.1:c.*443A>C	ENSP00000510658.1:n.*443A>C
ENST00000690544.1:c.*2451A>C	ENSP00000508989.1:n.*2451A>C
ENST00000358913.10:c.3180A>C MANE Select	ENSP00000351790.5:p.Glu1060Asp
ENST00000354393.6:c.2355A>C	ENSP00000346369.2:p.Glu785Asp
ENST00000358913.9:c.3180A>C	ENSP00000351790.5:p.Glu1060Asp
ENST00000540630.5:c.3180A>C	ENSP00000441668.2:p.Glu1060Asp
ENST00000613327.4:c.2298A>C	ENSP00000480757.1:p.Glu766Asp
NM_001256267.1:c.3180A>C	NP_001243196.1:p.Glu1060Asp
NM_001256268.1:c.2298A>C	NP_001243197.1:p.Glu766Asp
NM_032578.3:c.3180A>C , LRG_410t1:c.3180A>C	NP_115967.2:p.Glu1060Asp
NR_045662.3:n.2607A>C
NR_045663.3:n.3309A>C
XM_006718043.2:c.3234A>C	XP_006718106.1:p.Glu1078Asp
XM_011540292.1:c.3210A>C	XP_011538594.1:p.Glu1070Asp
XM_017016833.1:c.3258A>C	XP_016872322.1:p.Glu1086Asp
XM_017016834.2:c.3180A>C	XP_016872323.1:p.Glu1060Asp
XM_024448236.1:c.2058A>C	XP_024304004.1:p.Glu686Asp
NR_045662.4:n.2717A>C
NR_045663.4:n.3254A>C
NM_001256267.2:c.3180A>C	NP_001243196.1:p.Glu1060Asp
NM_001256268.2:c.2298A>C	NP_001243197.1:p.Glu766Asp
NM_032578.4:c.3180A>C MANE Select	NP_115967.2:p.Glu1060Asp