Canonical Allele Identifier: CA667799867
Gene: MYPN HGNC NCBI

Linked Data

dbSNP Id: rs1354355325

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68199364T>C , CM000672.2:g.68199364T>C GRCh38
NC_000010.10:g.69959121T>C , CM000672.1:g.69959121T>C GRCh37
NC_000010.9:g.69629127T>C NCBI36
NG_032118.1:g.98248T>C , LRG_410:g.98248T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.2461-4T>C ENSP00000346369.2:n.2461-4T>C
ENST00000540630.6:c.3340-4T>C ENSP00000441668.3:n.3340-4T>C
ENST00000613327.5:c.3286-4T>C ENSP00000480757.2:n.3286-4T>C
ENST00000688812.1:c.*549-4T>C ENSP00000510658.1:n.*549-4T>C
ENST00000690544.1:c.*2557-4T>C ENSP00000508989.1:n.*2557-4T>C
ENST00000358913.10:c.3286-4T>C MANE Select ENSP00000351790.5:n.3286-4T>C
ENST00000354393.6:c.2461-4T>C ENSP00000346369.2:n.2461-4T>C
ENST00000358913.9:c.3286-4T>C ENSP00000351790.5:n.3286-4T>C
ENST00000540630.5:c.3286-4T>C ENSP00000441668.2:n.3286-4T>C
ENST00000613327.4:c.2404-4T>C ENSP00000480757.1:n.2404-4T>C
NM_001256267.1:c.3286-4T>C NP_001243196.1:n.3286-4T>C
NM_001256268.1:c.2404-4T>C NP_001243197.1:n.2404-4T>C
NM_032578.3:c.3286-4T>C , LRG_410t1:c.3286-4T>C NP_115967.2:n.3286-4T>C
NR_045662.3:n.2713-4T>C
NR_045663.3:n.3415-4T>C
XM_006718043.2:c.3340-4T>C XP_006718106.1:n.3340-4T>C
XM_011540292.1:c.3316-4T>C XP_011538594.1:n.3316-4T>C
XR_946029.1:n.1804-89A>G
XM_017016833.1:c.3364-4T>C XP_016872322.1:n.3364-4T>C
XM_017016834.2:c.3286-4T>C XP_016872323.1:n.3286-4T>C
XM_024448236.1:c.2164-4T>C XP_024304004.1:n.2164-4T>C
NR_045662.4:n.2823-4T>C
NR_045663.4:n.3360-4T>C
NM_001256267.2:c.3286-4T>C NP_001243196.1:n.3286-4T>C
NM_001256268.2:c.2404-4T>C NP_001243197.1:n.2404-4T>C
NM_032578.4:c.3286-4T>C MANE Select NP_115967.2:n.3286-4T>C