Canonical Allele Identifier: CA1557861673

Gene: JMY

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.79262117_79262118delinsAC , CM000667.2:g.79262117_79262118delinsAC	GRCh38
NC_000005.9:g.78557940_78557941delinsAC , CM000667.1:g.78557940_78557941delinsAC	GRCh37
NC_000005.8:g.78593696_78593697delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396137.5:c.1033-15793_1033-15792delinsAC MANE Select	ENSP00000379441.4:n.1033-15793_1033-15792delinsAC
ENST00000396137.4:c.1033-15793_1033-15792delinsAC	ENSP00000379441.4:n.1033-15793_1033-15792delinsAC
NM_152405.4:c.1033-15793_1033-15792delinsAC	NP_689618.4:n.1033-15793_1033-15792delinsAC
XM_005248430.1:c.1033-15793_1033-15792delinsAC	XP_005248487.1:n.1033-15793_1033-15792delinsAC
XM_011543155.1:c.1033-15793_1033-15792delinsAC	XP_011541457.1:n.1033-15793_1033-15792delinsAC
XM_005248430.3:c.1033-15793_1033-15792delinsAC	XP_005248487.1:n.1033-15793_1033-15792delinsAC
XM_011543155.3:c.1033-15793_1033-15792delinsAC	XP_011541457.1:n.1033-15793_1033-15792delinsAC
NM_152405.5:c.1033-15793_1033-15792delinsAC MANE Select	NP_689618.4:n.1033-15793_1033-15792delinsAC