Canonical Allele Identifier: CA376840378

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926279A>G (hg19) ; chr10:g.68166522A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166522A>G , CM000672.2:g.68166522A>G	GRCh38
NC_000010.10:g.69926279A>G , CM000672.1:g.69926279A>G	GRCh37
NC_000010.9:g.69596285A>G	NCBI36
NG_032118.1:g.65406A>G , LRG_410:g.65406A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1004A>G	ENSP00000346369.2:p.Glu335Gly
ENST00000373675.4:c.1829A>G	ENSP00000362779.4:p.Glu610Gly
ENST00000540630.6:c.1883A>G	ENSP00000441668.3:p.Glu628Gly
ENST00000613327.5:c.1829A>G	ENSP00000480757.2:p.Glu610Gly
ENST00000687572.1:c.707A>G	ENSP00000510427.1:p.Glu236Gly
ENST00000688812.1:c.1805A>G	ENSP00000510658.1:p.Glu602Gly
ENST00000690544.1:c.*1100A>G	ENSP00000508989.1:n.*1100A>G
ENST00000358913.10:c.1829A>G MANE Select	ENSP00000351790.5:p.Glu610Gly
ENST00000354393.6:c.1004A>G	ENSP00000346369.2:p.Glu335Gly
ENST00000358913.9:c.1829A>G	ENSP00000351790.5:p.Glu610Gly
ENST00000540630.5:c.1829A>G	ENSP00000441668.2:p.Glu610Gly
ENST00000613327.4:c.947A>G	ENSP00000480757.1:p.Glu316Gly
NM_001256267.1:c.1829A>G	NP_001243196.1:p.Glu610Gly
NM_001256268.1:c.947A>G	NP_001243197.1:p.Glu316Gly
NM_032578.3:c.1829A>G , LRG_410t1:c.1829A>G	NP_115967.2:p.Glu610Gly
NR_045662.3:n.1256A>G
NR_045663.3:n.2097A>G
XM_006718043.2:c.1883A>G	XP_006718106.1:p.Glu628Gly
XM_011540292.1:c.1859A>G	XP_011538594.1:p.Glu620Gly
XM_017016833.1:c.1907A>G	XP_016872322.1:p.Glu636Gly
XM_017016834.2:c.1829A>G	XP_016872323.1:p.Glu610Gly
XM_024448236.1:c.707A>G	XP_024304004.1:p.Glu236Gly
NR_045662.4:n.1366A>G
NR_045663.4:n.2042A>G
NM_001256267.2:c.1829A>G	NP_001243196.1:p.Glu610Gly
NM_001256268.2:c.947A>G	NP_001243197.1:p.Glu316Gly
NM_032578.4:c.1829A>G MANE Select	NP_115967.2:p.Glu610Gly