Canonical Allele Identifier: CA5522672
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 691723
dbSNP Id: rs754064567

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68166569G>A , CM000672.2:g.68166569G>A GRCh38
NC_000010.10:g.69926326G>A , CM000672.1:g.69926326G>A GRCh37
NC_000010.9:g.69596332G>A NCBI36
NG_032118.1:g.65453G>A , LRG_410:g.65453G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.1051G>A ENSP00000346369.2:p.Asp351Asn
ENST00000373675.4:c.1876G>A ENSP00000362779.4:p.Asp626Asn
ENST00000540630.6:c.1930G>A ENSP00000441668.3:p.Asp644Asn
ENST00000613327.5:c.1876G>A ENSP00000480757.2:p.Asp626Asn
ENST00000687572.1:c.754G>A ENSP00000510427.1:p.Asp252Asn
ENST00000688812.1:c.1852G>A ENSP00000510658.1:p.Asp618Asn
ENST00000690544.1:c.*1147G>A ENSP00000508989.1:n.*1147G>A
ENST00000358913.10:c.1876G>A MANE Select ENSP00000351790.5:p.Asp626Asn
ENST00000354393.6:c.1051G>A ENSP00000346369.2:p.Asp351Asn
ENST00000358913.9:c.1876G>A ENSP00000351790.5:p.Asp626Asn
ENST00000540630.5:c.1876G>A ENSP00000441668.2:p.Asp626Asn
ENST00000613327.4:c.994G>A ENSP00000480757.1:p.Asp332Asn
NM_001256267.1:c.1876G>A NP_001243196.1:p.Asp626Asn
NM_001256268.1:c.994G>A NP_001243197.1:p.Asp332Asn
NM_032578.3:c.1876G>A , LRG_410t1:c.1876G>A NP_115967.2:p.Asp626Asn
NR_045662.3:n.1303G>A
NR_045663.3:n.2144G>A
XM_006718043.2:c.1930G>A XP_006718106.1:p.Asp644Asn
XM_011540292.1:c.1906G>A XP_011538594.1:p.Asp636Asn
XM_017016833.1:c.1954G>A XP_016872322.1:p.Asp652Asn
XM_017016834.2:c.1876G>A XP_016872323.1:p.Asp626Asn
XM_024448236.1:c.754G>A XP_024304004.1:p.Asp252Asn
NR_045662.4:n.1413G>A
NR_045663.4:n.2089G>A
NM_001256267.2:c.1876G>A NP_001243196.1:p.Asp626Asn
NM_001256268.2:c.994G>A NP_001243197.1:p.Asp332Asn
NM_032578.4:c.1876G>A MANE Select NP_115967.2:p.Asp626Asn