Canonical Allele Identifier: CA376840533

Gene: MYPN

Linked Data

• ClinVar Variation Id: 1414485
• ClinVar RCV Id: RCV001945308
• dbSNP Id: rs2134169106
• MyVariant Identifiers: chr10:g.69926315A>G (hg19) ; chr10:g.68166558A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166558A>G , CM000672.2:g.68166558A>G	GRCh38
NC_000010.10:g.69926315A>G , CM000672.1:g.69926315A>G	GRCh37
NC_000010.9:g.69596321A>G	NCBI36
NG_032118.1:g.65442A>G , LRG_410:g.65442A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1040A>G	ENSP00000346369.2:p.Gln347Arg
ENST00000373675.4:c.1865A>G	ENSP00000362779.4:p.Gln622Arg
ENST00000540630.6:c.1919A>G	ENSP00000441668.3:p.Gln640Arg
ENST00000613327.5:c.1865A>G	ENSP00000480757.2:p.Gln622Arg
ENST00000687572.1:c.743A>G	ENSP00000510427.1:p.Gln248Arg
ENST00000688812.1:c.1841A>G	ENSP00000510658.1:p.Gln614Arg
ENST00000690544.1:c.*1136A>G	ENSP00000508989.1:n.*1136A>G
ENST00000358913.10:c.1865A>G MANE Select	ENSP00000351790.5:p.Gln622Arg
ENST00000354393.6:c.1040A>G	ENSP00000346369.2:p.Gln347Arg
ENST00000358913.9:c.1865A>G	ENSP00000351790.5:p.Gln622Arg
ENST00000540630.5:c.1865A>G	ENSP00000441668.2:p.Gln622Arg
ENST00000613327.4:c.983A>G	ENSP00000480757.1:p.Gln328Arg
NM_001256267.1:c.1865A>G	NP_001243196.1:p.Gln622Arg
NM_001256268.1:c.983A>G	NP_001243197.1:p.Gln328Arg
NM_032578.3:c.1865A>G , LRG_410t1:c.1865A>G	NP_115967.2:p.Gln622Arg
NR_045662.3:n.1292A>G
NR_045663.3:n.2133A>G
XM_006718043.2:c.1919A>G	XP_006718106.1:p.Gln640Arg
XM_011540292.1:c.1895A>G	XP_011538594.1:p.Gln632Arg
XM_017016833.1:c.1943A>G	XP_016872322.1:p.Gln648Arg
XM_017016834.2:c.1865A>G	XP_016872323.1:p.Gln622Arg
XM_024448236.1:c.743A>G	XP_024304004.1:p.Gln248Arg
NR_045662.4:n.1402A>G
NR_045663.4:n.2078A>G
NM_001256267.2:c.1865A>G	NP_001243196.1:p.Gln622Arg
NM_001256268.2:c.983A>G	NP_001243197.1:p.Gln328Arg
NM_032578.4:c.1865A>G MANE Select	NP_115967.2:p.Gln622Arg