Canonical Allele Identifier: CA376839287

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926058G>C (hg19) ; chr10:g.68166301G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166301G>C , CM000672.2:g.68166301G>C	GRCh38
NC_000010.10:g.69926058G>C , CM000672.1:g.69926058G>C	GRCh37
NC_000010.9:g.69596064G>C	NCBI36
NG_032118.1:g.65185G>C , LRG_410:g.65185G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.783G>C	ENSP00000346369.2:p.Glu261Asp
ENST00000373675.4:c.1608G>C	ENSP00000362779.4:p.Glu536Asp
ENST00000540630.6:c.1662G>C	ENSP00000441668.3:p.Glu554Asp
ENST00000613327.5:c.1608G>C	ENSP00000480757.2:p.Glu536Asp
ENST00000687572.1:c.486G>C	ENSP00000510427.1:p.Glu162Asp
ENST00000687705.1:c.*1857G>C	ENSP00000509639.1:n.*1857G>C
ENST00000688812.1:c.1584G>C	ENSP00000510658.1:p.Glu528Asp
ENST00000689002.1:n.660G>C
ENST00000690544.1:c.*879G>C	ENSP00000508989.1:n.*879G>C
ENST00000358913.10:c.1608G>C MANE Select	ENSP00000351790.5:p.Glu536Asp
ENST00000354393.6:c.783G>C	ENSP00000346369.2:p.Glu261Asp
ENST00000358913.9:c.1608G>C	ENSP00000351790.5:p.Glu536Asp
ENST00000540630.5:c.1608G>C	ENSP00000441668.2:p.Glu536Asp
ENST00000613327.4:c.726G>C	ENSP00000480757.1:p.Glu242Asp
NM_001256267.1:c.1608G>C	NP_001243196.1:p.Glu536Asp
NM_001256268.1:c.726G>C	NP_001243197.1:p.Glu242Asp
NM_032578.3:c.1608G>C , LRG_410t1:c.1608G>C	NP_115967.2:p.Glu536Asp
NR_045662.3:n.1035G>C
NR_045663.3:n.1876G>C
XM_006718043.2:c.1662G>C	XP_006718106.1:p.Glu554Asp
XM_011540292.1:c.1638G>C	XP_011538594.1:p.Glu546Asp
XM_017016833.1:c.1686G>C	XP_016872322.1:p.Glu562Asp
XM_017016834.2:c.1608G>C	XP_016872323.1:p.Glu536Asp
XM_024448236.1:c.486G>C	XP_024304004.1:p.Glu162Asp
NR_045662.4:n.1145G>C
NR_045663.4:n.1821G>C
NM_001256267.2:c.1608G>C	NP_001243196.1:p.Glu536Asp
NM_001256268.2:c.726G>C	NP_001243197.1:p.Glu242Asp
NM_032578.4:c.1608G>C MANE Select	NP_115967.2:p.Glu536Asp