Canonical Allele Identifier: CA2609372308

Gene: MYPN

Linked Data

• gnomAD v4: 10-68165813-TGAGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165815_68165819del , CM000672.2:g.68165815_68165819del	GRCh38
NC_000010.10:g.69925572_69925576del , CM000672.1:g.69925572_69925576del	GRCh37
NC_000010.9:g.69595578_69595582del	NCBI36
NG_032118.1:g.64699_64703del , LRG_410:g.64699_64703del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.772_775+1del
ENST00000373675.4:c.1597_1600+1del
ENST00000540630.6:c.1651_1654+1del
ENST00000613327.5:c.1597_1600+1del
ENST00000687572.1:c.475_478+1del
ENST00000687705.1:c.*1846_*1849+1del
ENST00000688812.1:c.1573_1576+1del
ENST00000689002.1:n.649_652+1del
ENST00000690544.1:c.*868_*871+1del
ENST00000358913.10:c.1597_1600+1del
ENST00000354393.6:c.772_775+1del
ENST00000358913.9:c.1597_1600+1del
ENST00000540630.5:c.1597_1600+1del
ENST00000613327.4:c.715_718+1del
NM_001256267.1:c.1597_1600+1del
NM_001256268.1:c.715_718+1del
NM_032578.3:c.1597_1600+1del , LRG_410t1:c.1597_1600+1del
NR_045662.3:n.1024_1027+1del
NR_045663.3:n.1865_1868+1del
XM_006718043.2:c.1651_1654+1del
XM_011540292.1:c.1627_1630+1del
XM_017016833.1:c.1675_1678+1del
XM_017016834.2:c.1597_1600+1del
XM_024448236.1:c.475_478+1del
NR_045662.4:n.1134_1137+1del
NR_045663.4:n.1810_1813+1del
NM_001256267.2:c.1597_1600+1del
NM_001256268.2:c.715_718+1del
NM_032578.4:c.1597_1600+1del