Canonical Allele Identifier: CA376839862

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926162A>G (hg19) ; chr10:g.68166405A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166405A>G , CM000672.2:g.68166405A>G	GRCh38
NC_000010.10:g.69926162A>G , CM000672.1:g.69926162A>G	GRCh37
NC_000010.9:g.69596168A>G	NCBI36
NG_032118.1:g.65289A>G , LRG_410:g.65289A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.887A>G	ENSP00000346369.2:p.Glu296Gly
ENST00000373675.4:c.1712A>G	ENSP00000362779.4:p.Glu571Gly
ENST00000540630.6:c.1766A>G	ENSP00000441668.3:p.Glu589Gly
ENST00000613327.5:c.1712A>G	ENSP00000480757.2:p.Glu571Gly
ENST00000687572.1:c.590A>G	ENSP00000510427.1:p.Glu197Gly
ENST00000688812.1:c.1688A>G	ENSP00000510658.1:p.Glu563Gly
ENST00000689002.1:n.764A>G
ENST00000690544.1:c.*983A>G	ENSP00000508989.1:n.*983A>G
ENST00000358913.10:c.1712A>G MANE Select	ENSP00000351790.5:p.Glu571Gly
ENST00000354393.6:c.887A>G	ENSP00000346369.2:p.Glu296Gly
ENST00000358913.9:c.1712A>G	ENSP00000351790.5:p.Glu571Gly
ENST00000540630.5:c.1712A>G	ENSP00000441668.2:p.Glu571Gly
ENST00000613327.4:c.830A>G	ENSP00000480757.1:p.Glu277Gly
NM_001256267.1:c.1712A>G	NP_001243196.1:p.Glu571Gly
NM_001256268.1:c.830A>G	NP_001243197.1:p.Glu277Gly
NM_032578.3:c.1712A>G , LRG_410t1:c.1712A>G	NP_115967.2:p.Glu571Gly
NR_045662.3:n.1139A>G
NR_045663.3:n.1980A>G
XM_006718043.2:c.1766A>G	XP_006718106.1:p.Glu589Gly
XM_011540292.1:c.1742A>G	XP_011538594.1:p.Glu581Gly
XM_017016833.1:c.1790A>G	XP_016872322.1:p.Glu597Gly
XM_017016834.2:c.1712A>G	XP_016872323.1:p.Glu571Gly
XM_024448236.1:c.590A>G	XP_024304004.1:p.Glu197Gly
NR_045662.4:n.1249A>G
NR_045663.4:n.1925A>G
NM_001256267.2:c.1712A>G	NP_001243196.1:p.Glu571Gly
NM_001256268.2:c.830A>G	NP_001243197.1:p.Glu277Gly
NM_032578.4:c.1712A>G MANE Select	NP_115967.2:p.Glu571Gly