Canonical Allele Identifier: CA376859271

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69959252A>G (hg19) ; chr10:g.68199495A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199495A>G , CM000672.2:g.68199495A>G	GRCh38
NC_000010.10:g.69959252A>G , CM000672.1:g.69959252A>G	GRCh37
NC_000010.9:g.69629258A>G	NCBI36
NG_032118.1:g.98379A>G , LRG_410:g.98379A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2588A>G	ENSP00000346369.2:p.Gln863Arg
ENST00000540630.6:c.3467A>G	ENSP00000441668.3:p.Gln1156Arg
ENST00000613327.5:c.3413A>G	ENSP00000480757.2:p.Gln1138Arg
ENST00000688812.1:c.*676A>G	ENSP00000510658.1:n.*676A>G
ENST00000690544.1:c.*2684A>G	ENSP00000508989.1:n.*2684A>G
ENST00000358913.10:c.3413A>G MANE Select	ENSP00000351790.5:p.Gln1138Arg
ENST00000354393.6:c.2588A>G	ENSP00000346369.2:p.Gln863Arg
ENST00000358913.9:c.3413A>G	ENSP00000351790.5:p.Gln1138Arg
ENST00000540630.5:c.3413A>G	ENSP00000441668.2:p.Gln1138Arg
ENST00000613327.4:c.2531A>G	ENSP00000480757.1:p.Gln844Arg
NM_001256267.1:c.3413A>G	NP_001243196.1:p.Gln1138Arg
NM_001256268.1:c.2531A>G	NP_001243197.1:p.Gln844Arg
NM_032578.3:c.3413A>G , LRG_410t1:c.3413A>G	NP_115967.2:p.Gln1138Arg
NR_045662.3:n.2840A>G
NR_045663.3:n.3542A>G
XM_006718043.2:c.3467A>G	XP_006718106.1:p.Gln1156Arg
XM_011540292.1:c.3443A>G	XP_011538594.1:p.Gln1148Arg
XR_946029.1:n.1804-220T>C
XM_017016833.1:c.3491A>G	XP_016872322.1:p.Gln1164Arg
XM_017016834.2:c.3413A>G	XP_016872323.1:p.Gln1138Arg
XM_024448236.1:c.2291A>G	XP_024304004.1:p.Gln764Arg
NR_045662.4:n.2950A>G
NR_045663.4:n.3487A>G
NM_001256267.2:c.3413A>G	NP_001243196.1:p.Gln1138Arg
NM_001256268.2:c.2531A>G	NP_001243197.1:p.Gln844Arg
NM_032578.4:c.3413A>G MANE Select	NP_115967.2:p.Gln1138Arg