Canonical Allele Identifier: CA376839877

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926165A>G (hg19) ; chr10:g.68166408A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166408A>G , CM000672.2:g.68166408A>G	GRCh38
NC_000010.10:g.69926165A>G , CM000672.1:g.69926165A>G	GRCh37
NC_000010.9:g.69596171A>G	NCBI36
NG_032118.1:g.65292A>G , LRG_410:g.65292A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.890A>G	ENSP00000346369.2:p.Gln297Arg
ENST00000373675.4:c.1715A>G	ENSP00000362779.4:p.Gln572Arg
ENST00000540630.6:c.1769A>G	ENSP00000441668.3:p.Gln590Arg
ENST00000613327.5:c.1715A>G	ENSP00000480757.2:p.Gln572Arg
ENST00000687572.1:c.593A>G	ENSP00000510427.1:p.Gln198Arg
ENST00000688812.1:c.1691A>G	ENSP00000510658.1:p.Gln564Arg
ENST00000689002.1:n.767A>G
ENST00000690544.1:c.*986A>G	ENSP00000508989.1:n.*986A>G
ENST00000358913.10:c.1715A>G MANE Select	ENSP00000351790.5:p.Gln572Arg
ENST00000354393.6:c.890A>G	ENSP00000346369.2:p.Gln297Arg
ENST00000358913.9:c.1715A>G	ENSP00000351790.5:p.Gln572Arg
ENST00000540630.5:c.1715A>G	ENSP00000441668.2:p.Gln572Arg
ENST00000613327.4:c.833A>G	ENSP00000480757.1:p.Gln278Arg
NM_001256267.1:c.1715A>G	NP_001243196.1:p.Gln572Arg
NM_001256268.1:c.833A>G	NP_001243197.1:p.Gln278Arg
NM_032578.3:c.1715A>G , LRG_410t1:c.1715A>G	NP_115967.2:p.Gln572Arg
NR_045662.3:n.1142A>G
NR_045663.3:n.1983A>G
XM_006718043.2:c.1769A>G	XP_006718106.1:p.Gln590Arg
XM_011540292.1:c.1745A>G	XP_011538594.1:p.Gln582Arg
XM_017016833.1:c.1793A>G	XP_016872322.1:p.Gln598Arg
XM_017016834.2:c.1715A>G	XP_016872323.1:p.Gln572Arg
XM_024448236.1:c.593A>G	XP_024304004.1:p.Gln198Arg
NR_045662.4:n.1252A>G
NR_045663.4:n.1928A>G
NM_001256267.2:c.1715A>G	NP_001243196.1:p.Gln572Arg
NM_001256268.2:c.833A>G	NP_001243197.1:p.Gln278Arg
NM_032578.4:c.1715A>G MANE Select	NP_115967.2:p.Gln572Arg