Canonical Allele Identifier: CA1557861706
Gene: JMY HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79262176A= , CM000667.2:g.79262176A= GRCh38
NC_000005.9:g.78557999A= , CM000667.1:g.78557999A= GRCh37
NC_000005.8:g.78593755A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000396137.5:c.1033-15734A= MANE Select ENSP00000379441.4:n.1033-15734A=
ENST00000396137.4:c.1033-15734A= ENSP00000379441.4:n.1033-15734A=
NM_152405.4:c.1033-15734A= NP_689618.4:n.1033-15734A=
XM_005248430.1:c.1033-15734A= XP_005248487.1:n.1033-15734A=
XM_011543155.1:c.1033-15734A= XP_011541457.1:n.1033-15734A=
XM_005248430.3:c.1033-15734A= XP_005248487.1:n.1033-15734A=
XM_011543155.3:c.1033-15734A= XP_011541457.1:n.1033-15734A=
NM_152405.5:c.1033-15734A= MANE Select NP_689618.4:n.1033-15734A=
Search 100 bp 5'
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