Canonical Allele Identifier: CA1557861697

Gene: JMY

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.79262157C= , CM000667.2:g.79262157C=	GRCh38
NC_000005.9:g.78557980C= , CM000667.1:g.78557980C=	GRCh37
NC_000005.8:g.78593736C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396137.5:c.1033-15753C= MANE Select	ENSP00000379441.4:n.1033-15753C=
ENST00000396137.4:c.1033-15753C=	ENSP00000379441.4:n.1033-15753C=
NM_152405.4:c.1033-15753C=	NP_689618.4:n.1033-15753C=
XM_005248430.1:c.1033-15753C=	XP_005248487.1:n.1033-15753C=
XM_011543155.1:c.1033-15753C=	XP_011541457.1:n.1033-15753C=
XM_005248430.3:c.1033-15753C=	XP_005248487.1:n.1033-15753C=
XM_011543155.3:c.1033-15753C=	XP_011541457.1:n.1033-15753C=
NM_152405.5:c.1033-15753C= MANE Select	NP_689618.4:n.1033-15753C=