Canonical Allele Identifier: CA5522949
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 431886
dbSNP Id: rs201975081
COSMIC: COSM919664

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68195477A>G , CM000672.2:g.68195477A>G GRCh38
NC_000010.10:g.69955234A>G , CM000672.1:g.69955234A>G GRCh37
NC_000010.9:g.69625240A>G NCBI36
NG_032118.1:g.94361A>G , LRG_410:g.94361A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.2278A>G ENSP00000346369.2:p.Met760Val
ENST00000540630.6:c.3157A>G ENSP00000441668.3:p.Met1053Val
ENST00000613327.5:c.3103A>G ENSP00000480757.2:p.Met1035Val
ENST00000688812.1:c.*366A>G ENSP00000510658.1:n.*366A>G
ENST00000690544.1:c.*2374A>G ENSP00000508989.1:n.*2374A>G
ENST00000358913.10:c.3103A>G MANE Select ENSP00000351790.5:p.Met1035Val
ENST00000354393.6:c.2278A>G ENSP00000346369.2:p.Met760Val
ENST00000358913.9:c.3103A>G ENSP00000351790.5:p.Met1035Val
ENST00000540630.5:c.3103A>G ENSP00000441668.2:p.Met1035Val
ENST00000613327.4:c.2221A>G ENSP00000480757.1:p.Met741Val
NM_001256267.1:c.3103A>G NP_001243196.1:p.Met1035Val
NM_001256268.1:c.2221A>G NP_001243197.1:p.Met741Val
NM_032578.3:c.3103A>G , LRG_410t1:c.3103A>G NP_115967.2:p.Met1035Val
NR_045662.3:n.2530A>G
NR_045663.3:n.3232A>G
XM_006718043.2:c.3157A>G XP_006718106.1:p.Met1053Val
XM_011540292.1:c.3133A>G XP_011538594.1:p.Met1045Val
XM_017016833.1:c.3181A>G XP_016872322.1:p.Met1061Val
XM_017016834.2:c.3103A>G XP_016872323.1:p.Met1035Val
XM_024448236.1:c.1981A>G XP_024304004.1:p.Met661Val
NR_045662.4:n.2640A>G
NR_045663.4:n.3177A>G
NM_001256267.2:c.3103A>G NP_001243196.1:p.Met1035Val
NM_001256268.2:c.2221A>G NP_001243197.1:p.Met741Val
NM_032578.4:c.3103A>G MANE Select NP_115967.2:p.Met1035Val