Canonical Allele Identifier: CA376840676

Gene: MYPN

Linked Data

• MyVariant Identifiers: chr10:g.69926347A>T (hg19) ; chr10:g.68166590A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166590A>T , CM000672.2:g.68166590A>T	GRCh38
NC_000010.10:g.69926347A>T , CM000672.1:g.69926347A>T	GRCh37
NC_000010.9:g.69596353A>T	NCBI36
NG_032118.1:g.65474A>T , LRG_410:g.65474A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1072A>T	ENSP00000346369.2:p.Asn358Tyr
ENST00000373675.4:c.1897A>T	ENSP00000362779.4:p.Asn633Tyr
ENST00000540630.6:c.1951A>T	ENSP00000441668.3:p.Asn651Tyr
ENST00000613327.5:c.1897A>T	ENSP00000480757.2:p.Asn633Tyr
ENST00000687572.1:c.775A>T	ENSP00000510427.1:p.Asn259Tyr
ENST00000688812.1:c.1873A>T	ENSP00000510658.1:p.Asn625Tyr
ENST00000690544.1:c.*1168A>T	ENSP00000508989.1:n.*1168A>T
ENST00000358913.10:c.1897A>T MANE Select	ENSP00000351790.5:p.Asn633Tyr
ENST00000354393.6:c.1072A>T	ENSP00000346369.2:p.Asn358Tyr
ENST00000358913.9:c.1897A>T	ENSP00000351790.5:p.Asn633Tyr
ENST00000540630.5:c.1897A>T	ENSP00000441668.2:p.Asn633Tyr
ENST00000613327.4:c.1015A>T	ENSP00000480757.1:p.Asn339Tyr
NM_001256267.1:c.1897A>T	NP_001243196.1:p.Asn633Tyr
NM_001256268.1:c.1015A>T	NP_001243197.1:p.Asn339Tyr
NM_032578.3:c.1897A>T , LRG_410t1:c.1897A>T	NP_115967.2:p.Asn633Tyr
NR_045662.3:n.1324A>T
NR_045663.3:n.2165A>T
XM_006718043.2:c.1951A>T	XP_006718106.1:p.Asn651Tyr
XM_011540292.1:c.1927A>T	XP_011538594.1:p.Asn643Tyr
XM_017016833.1:c.1975A>T	XP_016872322.1:p.Asn659Tyr
XM_017016834.2:c.1897A>T	XP_016872323.1:p.Asn633Tyr
XM_024448236.1:c.775A>T	XP_024304004.1:p.Asn259Tyr
NR_045662.4:n.1434A>T
NR_045663.4:n.2110A>T
NM_001256267.2:c.1897A>T	NP_001243196.1:p.Asn633Tyr
NM_001256268.2:c.1015A>T	NP_001243197.1:p.Asn339Tyr
NM_032578.4:c.1897A>T MANE Select	NP_115967.2:p.Asn633Tyr