Canonical Allele Identifier: CA376839703

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926126A>G (hg19) ; chr10:g.68166369A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166369A>G , CM000672.2:g.68166369A>G	GRCh38
NC_000010.10:g.69926126A>G , CM000672.1:g.69926126A>G	GRCh37
NC_000010.9:g.69596132A>G	NCBI36
NG_032118.1:g.65253A>G , LRG_410:g.65253A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.851A>G	ENSP00000346369.2:p.Gln284Arg
ENST00000373675.4:c.1676A>G	ENSP00000362779.4:p.Gln559Arg
ENST00000540630.6:c.1730A>G	ENSP00000441668.3:p.Gln577Arg
ENST00000613327.5:c.1676A>G	ENSP00000480757.2:p.Gln559Arg
ENST00000687572.1:c.554A>G	ENSP00000510427.1:p.Gln185Arg
ENST00000687705.1:c.*1925A>G	ENSP00000509639.1:n.*1925A>G
ENST00000688812.1:c.1652A>G	ENSP00000510658.1:p.Gln551Arg
ENST00000689002.1:n.728A>G
ENST00000690544.1:c.*947A>G	ENSP00000508989.1:n.*947A>G
ENST00000358913.10:c.1676A>G MANE Select	ENSP00000351790.5:p.Gln559Arg
ENST00000354393.6:c.851A>G	ENSP00000346369.2:p.Gln284Arg
ENST00000358913.9:c.1676A>G	ENSP00000351790.5:p.Gln559Arg
ENST00000540630.5:c.1676A>G	ENSP00000441668.2:p.Gln559Arg
ENST00000613327.4:c.794A>G	ENSP00000480757.1:p.Gln265Arg
NM_001256267.1:c.1676A>G	NP_001243196.1:p.Gln559Arg
NM_001256268.1:c.794A>G	NP_001243197.1:p.Gln265Arg
NM_032578.3:c.1676A>G , LRG_410t1:c.1676A>G	NP_115967.2:p.Gln559Arg
NR_045662.3:n.1103A>G
NR_045663.3:n.1944A>G
XM_006718043.2:c.1730A>G	XP_006718106.1:p.Gln577Arg
XM_011540292.1:c.1706A>G	XP_011538594.1:p.Gln569Arg
XM_017016833.1:c.1754A>G	XP_016872322.1:p.Gln585Arg
XM_017016834.2:c.1676A>G	XP_016872323.1:p.Gln559Arg
XM_024448236.1:c.554A>G	XP_024304004.1:p.Gln185Arg
NR_045662.4:n.1213A>G
NR_045663.4:n.1889A>G
NM_001256267.2:c.1676A>G	NP_001243196.1:p.Gln559Arg
NM_001256268.2:c.794A>G	NP_001243197.1:p.Gln265Arg
NM_032578.4:c.1676A>G MANE Select	NP_115967.2:p.Gln559Arg