Canonical Allele Identifier: CA469812441
Gene: MYPN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.69959220A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68199463A>C , CM000672.2:g.68199463A>C GRCh38
NC_000010.10:g.69959220A>C , CM000672.1:g.69959220A>C GRCh37
NC_000010.9:g.69629226A>C NCBI36
NG_032118.1:g.98347A>C , LRG_410:g.98347A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.2556A>C ENSP00000346369.2:p.Gly852=
ENST00000540630.6:c.3435A>C ENSP00000441668.3:p.Gly1145=
ENST00000613327.5:c.3381A>C ENSP00000480757.2:p.Gly1127=
ENST00000688812.1:c.*644A>C ENSP00000510658.1:n.*644A>C
ENST00000690544.1:c.*2652A>C ENSP00000508989.1:n.*2652A>C
ENST00000358913.10:c.3381A>C MANE Select ENSP00000351790.5:p.Gly1127=
ENST00000354393.6:c.2556A>C ENSP00000346369.2:p.Gly852=
ENST00000358913.9:c.3381A>C ENSP00000351790.5:p.Gly1127=
ENST00000540630.5:c.3381A>C ENSP00000441668.2:p.Gly1127=
ENST00000613327.4:c.2499A>C ENSP00000480757.1:p.Gly833=
NM_001256267.1:c.3381A>C NP_001243196.1:p.Gly1127=
NM_001256268.1:c.2499A>C NP_001243197.1:p.Gly833=
NM_032578.3:c.3381A>C , LRG_410t1:c.3381A>C NP_115967.2:p.Gly1127=
NR_045662.3:n.2808A>C
NR_045663.3:n.3510A>C
XM_006718043.2:c.3435A>C XP_006718106.1:p.Gly1145=
XM_011540292.1:c.3411A>C XP_011538594.1:p.Gly1137=
XR_946029.1:n.1804-188T>G
XM_017016833.1:c.3459A>C XP_016872322.1:p.Gly1153=
XM_017016834.2:c.3381A>C XP_016872323.1:p.Gly1127=
XM_024448236.1:c.2259A>C XP_024304004.1:p.Gly753=
NR_045662.4:n.2918A>C
NR_045663.4:n.3455A>C
NM_001256267.2:c.3381A>C NP_001243196.1:p.Gly1127=
NM_001256268.2:c.2499A>C NP_001243197.1:p.Gly833=
NM_032578.4:c.3381A>C MANE Select NP_115967.2:p.Gly1127=