Canonical Allele Identifier: CA376840673
Gene: MYPN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68166588T>C , CM000672.2:g.68166588T>C GRCh38
NC_000010.10:g.69926345T>C , CM000672.1:g.69926345T>C GRCh37
NC_000010.9:g.69596351T>C NCBI36
NG_032118.1:g.65472T>C , LRG_410:g.65472T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.1070T>C ENSP00000346369.2:p.Phe357Ser
ENST00000373675.4:c.1895T>C ENSP00000362779.4:p.Phe632Ser
ENST00000540630.6:c.1949T>C ENSP00000441668.3:p.Phe650Ser
ENST00000613327.5:c.1895T>C ENSP00000480757.2:p.Phe632Ser
ENST00000687572.1:c.773T>C ENSP00000510427.1:p.Phe258Ser
ENST00000688812.1:c.1871T>C ENSP00000510658.1:p.Phe624Ser
ENST00000690544.1:c.*1166T>C ENSP00000508989.1:n.*1166T>C
ENST00000358913.10:c.1895T>C MANE Select ENSP00000351790.5:p.Phe632Ser
ENST00000354393.6:c.1070T>C ENSP00000346369.2:p.Phe357Ser
ENST00000358913.9:c.1895T>C ENSP00000351790.5:p.Phe632Ser
ENST00000540630.5:c.1895T>C ENSP00000441668.2:p.Phe632Ser
ENST00000613327.4:c.1013T>C ENSP00000480757.1:p.Phe338Ser
NM_001256267.1:c.1895T>C NP_001243196.1:p.Phe632Ser
NM_001256268.1:c.1013T>C NP_001243197.1:p.Phe338Ser
NM_032578.3:c.1895T>C , LRG_410t1:c.1895T>C NP_115967.2:p.Phe632Ser
NR_045662.3:n.1322T>C
NR_045663.3:n.2163T>C
XM_006718043.2:c.1949T>C XP_006718106.1:p.Phe650Ser
XM_011540292.1:c.1925T>C XP_011538594.1:p.Phe642Ser
XM_017016833.1:c.1973T>C XP_016872322.1:p.Phe658Ser
XM_017016834.2:c.1895T>C XP_016872323.1:p.Phe632Ser
XM_024448236.1:c.773T>C XP_024304004.1:p.Phe258Ser
NR_045662.4:n.1432T>C
NR_045663.4:n.2108T>C
NM_001256267.2:c.1895T>C NP_001243196.1:p.Phe632Ser
NM_001256268.2:c.1013T>C NP_001243197.1:p.Phe338Ser
NM_032578.4:c.1895T>C MANE Select NP_115967.2:p.Phe632Ser