Canonical Allele Identifier: CA376858861
Gene: MYPN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68199371A>G , CM000672.2:g.68199371A>G GRCh38
NC_000010.10:g.69959128A>G , CM000672.1:g.69959128A>G GRCh37
NC_000010.9:g.69629134A>G NCBI36
NG_032118.1:g.98255A>G , LRG_410:g.98255A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.2464A>G ENSP00000346369.2:p.Ser822Gly
ENST00000540630.6:c.3343A>G ENSP00000441668.3:p.Ser1115Gly
ENST00000613327.5:c.3289A>G ENSP00000480757.2:p.Ser1097Gly
ENST00000688812.1:c.*552A>G ENSP00000510658.1:n.*552A>G
ENST00000690544.1:c.*2560A>G ENSP00000508989.1:n.*2560A>G
ENST00000358913.10:c.3289A>G MANE Select ENSP00000351790.5:p.Ser1097Gly
ENST00000354393.6:c.2464A>G ENSP00000346369.2:p.Ser822Gly
ENST00000358913.9:c.3289A>G ENSP00000351790.5:p.Ser1097Gly
ENST00000540630.5:c.3289A>G ENSP00000441668.2:p.Ser1097Gly
ENST00000613327.4:c.2407A>G ENSP00000480757.1:p.Ser803Gly
NM_001256267.1:c.3289A>G NP_001243196.1:p.Ser1097Gly
NM_001256268.1:c.2407A>G NP_001243197.1:p.Ser803Gly
NM_032578.3:c.3289A>G , LRG_410t1:c.3289A>G NP_115967.2:p.Ser1097Gly
NR_045662.3:n.2716A>G
NR_045663.3:n.3418A>G
XM_006718043.2:c.3343A>G XP_006718106.1:p.Ser1115Gly
XM_011540292.1:c.3319A>G XP_011538594.1:p.Ser1107Gly
XR_946029.1:n.1804-96T>C
XM_017016833.1:c.3367A>G XP_016872322.1:p.Ser1123Gly
XM_017016834.2:c.3289A>G XP_016872323.1:p.Ser1097Gly
XM_024448236.1:c.2167A>G XP_024304004.1:p.Ser723Gly
NR_045662.4:n.2826A>G
NR_045663.4:n.3363A>G
NM_001256267.2:c.3289A>G NP_001243196.1:p.Ser1097Gly
NM_001256268.2:c.2407A>G NP_001243197.1:p.Ser803Gly
NM_032578.4:c.3289A>G MANE Select NP_115967.2:p.Ser1097Gly