Canonical Allele Identifier: CA376858842
Gene: MYPN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68199366A>T , CM000672.2:g.68199366A>T GRCh38
NC_000010.10:g.69959123A>T , CM000672.1:g.69959123A>T GRCh37
NC_000010.9:g.69629129A>T NCBI36
NG_032118.1:g.98250A>T , LRG_410:g.98250A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.2461-2A>T ENSP00000346369.2:n.2461-2A>T
ENST00000540630.6:c.3340-2A>T ENSP00000441668.3:n.3340-2A>T
ENST00000613327.5:c.3286-2A>T ENSP00000480757.2:n.3286-2A>T
ENST00000688812.1:c.*549-2A>T ENSP00000510658.1:n.*549-2A>T
ENST00000690544.1:c.*2557-2A>T ENSP00000508989.1:n.*2557-2A>T
ENST00000358913.10:c.3286-2A>T MANE Select ENSP00000351790.5:n.3286-2A>T
ENST00000354393.6:c.2461-2A>T ENSP00000346369.2:n.2461-2A>T
ENST00000358913.9:c.3286-2A>T ENSP00000351790.5:n.3286-2A>T
ENST00000540630.5:c.3286-2A>T ENSP00000441668.2:n.3286-2A>T
ENST00000613327.4:c.2404-2A>T ENSP00000480757.1:n.2404-2A>T
NM_001256267.1:c.3286-2A>T NP_001243196.1:n.3286-2A>T
NM_001256268.1:c.2404-2A>T NP_001243197.1:n.2404-2A>T
NM_032578.3:c.3286-2A>T , LRG_410t1:c.3286-2A>T NP_115967.2:n.3286-2A>T
NR_045662.3:n.2713-2A>T
NR_045663.3:n.3415-2A>T
XM_006718043.2:c.3340-2A>T XP_006718106.1:n.3340-2A>T
XM_011540292.1:c.3316-2A>T XP_011538594.1:n.3316-2A>T
XR_946029.1:n.1804-91T>A
XM_017016833.1:c.3364-2A>T XP_016872322.1:n.3364-2A>T
XM_017016834.2:c.3286-2A>T XP_016872323.1:n.3286-2A>T
XM_024448236.1:c.2164-2A>T XP_024304004.1:n.2164-2A>T
NR_045662.4:n.2823-2A>T
NR_045663.4:n.3360-2A>T
NM_001256267.2:c.3286-2A>T NP_001243196.1:n.3286-2A>T
NM_001256268.2:c.2404-2A>T NP_001243197.1:n.2404-2A>T
NM_032578.4:c.3286-2A>T MANE Select NP_115967.2:n.3286-2A>T