Canonical Allele Identifier: CA2556596097

Gene: JMY

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.79262037del , CM000667.2:g.79262037del	GRCh38
NC_000005.9:g.78557860del , CM000667.1:g.78557860del	GRCh37
NC_000005.8:g.78593616del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396137.5:c.1033-15873del MANE Select	ENSP00000379441.4:n.1033-15873del
ENST00000396137.4:c.1033-15873del	ENSP00000379441.4:n.1033-15873del
NM_152405.4:c.1033-15873del	NP_689618.4:n.1033-15873del
XM_005248430.1:c.1033-15873del	XP_005248487.1:n.1033-15873del
XM_011543155.1:c.1033-15873del	XP_011541457.1:n.1033-15873del
XM_005248430.3:c.1033-15873del	XP_005248487.1:n.1033-15873del
XM_011543155.3:c.1033-15873del	XP_011541457.1:n.1033-15873del
NM_152405.5:c.1033-15873del MANE Select	NP_689618.4:n.1033-15873del