Canonical Allele Identifier: CA1620559497

Gene: ILRUN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34651116G= , CM000668.2:g.34651116G=	GRCh38
NC_000006.11:g.34618893G= , CM000668.1:g.34618893G=	GRCh37
NC_000006.10:g.34726871G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374023.8:c.313+3509C= MANE Select	ENSP00000363135.3:n.313+3509C=
ENST00000374021.1:c.91+3509C=	ENSP00000363133.1:n.91+3509C=
ENST00000374023.7:c.313+3509C=	ENSP00000363135.3:n.313+3509C=
ENST00000374026.7:c.313+3509C=	ENSP00000363138.3:n.313+3509C=
NM_022758.5:c.313+3509C=	NP_073595.2:n.313+3509C=
NM_024294.3:c.313+3509C=	NP_077270.1:n.313+3509C=
XM_005249298.1:c.313+3509C=	XP_005249355.1:n.313+3509C=
XR_926300.1:n.512+3509C=
XM_005249298.3:c.313+3509C=	XP_005249355.1:n.313+3509C=
XR_926300.3:n.475+3509C=
NM_024294.4:c.313+3509C= MANE Select	NP_077270.1:n.313+3509C=
NM_022758.6:c.313+3509C=	NP_073595.2:n.313+3509C=