Canonical Allele Identifier: CA1917215804
Gene: MYPN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68166315A= , CM000672.2:g.68166315A= GRCh38
NC_000010.10:g.69926072A= , CM000672.1:g.69926072A= GRCh37
NC_000010.9:g.69596078A= NCBI36
NG_032118.1:g.65199A= , LRG_410:g.65199A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.797A= ENSP00000346369.2:p.Asn266=
ENST00000373675.4:c.1622A= ENSP00000362779.4:p.Asn541=
ENST00000540630.6:c.1676A= ENSP00000441668.3:p.Asn559=
ENST00000613327.5:c.1622A= ENSP00000480757.2:p.Asn541=
ENST00000687572.1:c.500A= ENSP00000510427.1:p.Asn167=
ENST00000687705.1:c.*1871A= ENSP00000509639.1:n.*1871A=
ENST00000688812.1:c.1598A= ENSP00000510658.1:p.Asn533=
ENST00000689002.1:n.674A=
ENST00000690544.1:c.*893A= ENSP00000508989.1:n.*893A=
ENST00000358913.10:c.1622A= MANE Select ENSP00000351790.5:p.Asn541=
ENST00000354393.6:c.797A= ENSP00000346369.2:p.Asn266=
ENST00000358913.9:c.1622A= ENSP00000351790.5:p.Asn541=
ENST00000540630.5:c.1622A= ENSP00000441668.2:p.Asn541=
ENST00000613327.4:c.740A= ENSP00000480757.1:p.Asn247=
NM_001256267.1:c.1622A= NP_001243196.1:p.Asn541=
NM_001256268.1:c.740A= NP_001243197.1:p.Asn247=
NM_032578.3:c.1622A= , LRG_410t1:c.1622A= NP_115967.2:p.Asn541=
NR_045662.3:n.1049A=
NR_045663.3:n.1890A=
XM_006718043.2:c.1676A= XP_006718106.1:p.Asn559=
XM_011540292.1:c.1652A= XP_011538594.1:p.Asn551=
XM_017016833.1:c.1700A= XP_016872322.1:p.Asn567=
XM_017016834.2:c.1622A= XP_016872323.1:p.Asn541=
XM_024448236.1:c.500A= XP_024304004.1:p.Asn167=
NR_045662.4:n.1159A=
NR_045663.4:n.1835A=
NM_001256267.2:c.1622A= NP_001243196.1:p.Asn541=
NM_001256268.2:c.740A= NP_001243197.1:p.Asn247=
NM_032578.4:c.1622A= MANE Select NP_115967.2:p.Asn541=