Canonical Allele Identifier: CA1917225532
Gene: MYPN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68195371C= , CM000672.2:g.68195371C= GRCh38
NC_000010.10:g.69955128C= , CM000672.1:g.69955128C= GRCh37
NC_000010.9:g.69625134C= NCBI36
NG_032118.1:g.94255C= , LRG_410:g.94255C=

Transcript Alleles

HGVS Amino-acid change
ENST00000354393.7:c.2251-79C= ENSP00000346369.2:n.2251-79C=
ENST00000540630.6:c.3130-79C= ENSP00000441668.3:n.3130-79C=
ENST00000613327.5:c.3076-79C= ENSP00000480757.2:n.3076-79C=
ENST00000688812.1:c.*339-79C= ENSP00000510658.1:n.*339-79C=
ENST00000690544.1:c.*2347-79C= ENSP00000508989.1:n.*2347-79C=
ENST00000358913.10:c.3076-79C= MANE Select ENSP00000351790.5:n.3076-79C=
ENST00000354393.6:c.2251-79C= ENSP00000346369.2:n.2251-79C=
ENST00000358913.9:c.3076-79C= ENSP00000351790.5:n.3076-79C=
ENST00000540630.5:c.3076-79C= ENSP00000441668.2:n.3076-79C=
ENST00000613327.4:c.2194-79C= ENSP00000480757.1:n.2194-79C=
NM_001256267.1:c.3076-79C= NP_001243196.1:n.3076-79C=
NM_001256268.1:c.2194-79C= NP_001243197.1:n.2194-79C=
NM_032578.3:c.3076-79C= , LRG_410t1:c.3076-79C= NP_115967.2:n.3076-79C=
NR_045662.3:n.2503-79C=
NR_045663.3:n.3205-79C=
XM_006718043.2:c.3130-79C= XP_006718106.1:n.3130-79C=
XM_011540292.1:c.3106-79C= XP_011538594.1:n.3106-79C=
XM_017016833.1:c.3154-79C= XP_016872322.1:n.3154-79C=
XM_017016834.2:c.3076-79C= XP_016872323.1:n.3076-79C=
XM_024448236.1:c.1954-79C= XP_024304004.1:n.1954-79C=
NR_045662.4:n.2613-79C=
NR_045663.4:n.3150-79C=
NM_001256267.2:c.3076-79C= NP_001243196.1:n.3076-79C=
NM_001256268.2:c.2194-79C= NP_001243197.1:n.2194-79C=
NM_032578.4:c.3076-79C= MANE Select NP_115967.2:n.3076-79C=