Canonical Allele Identifier: CA16044350
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 375565
ClinVar RCV Id: RCV000417065
dbSNP Id: rs1057519571

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68195448A>C , CM000672.2:g.68195448A>C GRCh38
NC_000010.10:g.69955205A>C , CM000672.1:g.69955205A>C GRCh37
NC_000010.9:g.69625211A>C NCBI36
NG_032118.1:g.94332A>C , LRG_410:g.94332A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000354393.7:c.2251-2A>C ENSP00000346369.2:n.2251-2A>C
ENST00000540630.6:c.3130-2A>C ENSP00000441668.3:n.3130-2A>C
ENST00000613327.5:c.3076-2A>C ENSP00000480757.2:n.3076-2A>C
ENST00000688812.1:c.*339-2A>C ENSP00000510658.1:n.*339-2A>C
ENST00000690544.1:c.*2347-2A>C ENSP00000508989.1:n.*2347-2A>C
ENST00000358913.10:c.3076-2A>C MANE Select ENSP00000351790.5:n.3076-2A>C
ENST00000354393.6:c.2251-2A>C ENSP00000346369.2:n.2251-2A>C
ENST00000358913.9:c.3076-2A>C ENSP00000351790.5:n.3076-2A>C
ENST00000540630.5:c.3076-2A>C ENSP00000441668.2:n.3076-2A>C
ENST00000613327.4:c.2194-2A>C ENSP00000480757.1:n.2194-2A>C
NM_001256267.1:c.3076-2A>C NP_001243196.1:n.3076-2A>C
NM_001256268.1:c.2194-2A>C NP_001243197.1:n.2194-2A>C
NM_032578.3:c.3076-2A>C , LRG_410t1:c.3076-2A>C NP_115967.2:n.3076-2A>C
NR_045662.3:n.2503-2A>C
NR_045663.3:n.3205-2A>C
XM_006718043.2:c.3130-2A>C XP_006718106.1:n.3130-2A>C
XM_011540292.1:c.3106-2A>C XP_011538594.1:n.3106-2A>C
XM_017016833.1:c.3154-2A>C XP_016872322.1:n.3154-2A>C
XM_017016834.2:c.3076-2A>C XP_016872323.1:n.3076-2A>C
XM_024448236.1:c.1954-2A>C XP_024304004.1:n.1954-2A>C
NR_045662.4:n.2613-2A>C
NR_045663.4:n.3150-2A>C
NM_001256267.2:c.3076-2A>C NP_001243196.1:n.3076-2A>C
NM_001256268.2:c.2194-2A>C NP_001243197.1:n.2194-2A>C
NM_032578.4:c.3076-2A>C MANE Select NP_115967.2:n.3076-2A>C