Canonical Allele Identifier: CA2270389394

Gene: MILR1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64462436_64462438delinsAGC , CM000679.2:g.64462436_64462438delinsAGC	GRCh38
NC_000017.9:g.59889014_59889016delinsAGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619286.5:c.763+1504_763+1506delinsAGC MANE Select	ENSP00000482801.1:n.763+1504_763+1506delinsAGC
ENST00000612535.4:c.493+1504_493+1506delinsAGC	ENSP00000477504.1:n.493+1504_493+1506delinsAGC
ENST00000615220.4:c.763+1504_763+1506delinsAGC	ENSP00000480749.1:n.763+1504_763+1506delinsAGC
ENST00000616498.4:c.478+1504_478+1506delinsAGC	ENSP00000481318.1:n.478+1504_478+1506delinsAGC
ENST00000619286.4:c.763+1504_763+1506delinsAGC	ENSP00000482801.1:n.763+1504_763+1506delinsAGC
NM_001085423.1:c.763+1504_763+1506delinsAGC	NP_001078892.1:n.763+1504_763+1506delinsAGC
NM_001291316.1:c.478+1504_478+1506delinsAGC	NP_001278245.1:n.478+1504_478+1506delinsAGC
NM_001291317.1:c.493+1504_493+1506delinsAGC	NP_001278246.1:n.493+1504_493+1506delinsAGC
XM_005276872.3:c.889+1504_889+1506delinsAGC	XP_005276929.1:n.889+1504_889+1506delinsAGC
XM_005276874.3:c.889+1504_889+1506delinsAGC	XP_005276931.1:n.889+1504_889+1506delinsAGC
XM_005276875.3:c.889+1504_889+1506delinsAGC	XP_005276932.1:n.889+1504_889+1506delinsAGC
XM_005276876.3:c.889+1504_889+1506delinsAGC	XP_005276933.1:n.889+1504_889+1506delinsAGC
XM_005276877.3:c.604+1504_604+1506delinsAGC	XP_005276934.1:n.604+1504_604+1506delinsAGC
XM_005276878.2:c.589+1504_589+1506delinsAGC	XP_005276935.1:n.589+1504_589+1506delinsAGC
XM_011524627.1:c.889+1504_889+1506delinsAGC	XP_011522929.1:n.889+1504_889+1506delinsAGC
XM_017024486.1:c.889+1504_889+1506delinsAGC	XP_016879975.1:n.889+1504_889+1506delinsAGC
XM_017024487.1:c.589+1504_589+1506delinsAGC	XP_016879976.1:n.589+1504_589+1506delinsAGC
XM_024450706.1:c.889+1504_889+1506delinsAGC	XP_024306474.1:n.889+1504_889+1506delinsAGC
XM_024450707.1:c.889+1504_889+1506delinsAGC	XP_024306475.1:n.889+1504_889+1506delinsAGC
XM_024450708.1:c.889+1504_889+1506delinsAGC	XP_024306476.1:n.889+1504_889+1506delinsAGC
XM_024450709.1:c.889+1504_889+1506delinsAGC	XP_024306477.1:n.889+1504_889+1506delinsAGC
XR_002957989.1:n.910+1504_910+1506delinsAGC
XR_002957990.1:n.910+1504_910+1506delinsAGC
NM_001085423.2:c.763+1504_763+1506delinsAGC MANE Select	NP_001078892.1:n.763+1504_763+1506delinsAGC
NM_001291316.2:c.478+1504_478+1506delinsAGC	NP_001278245.1:n.478+1504_478+1506delinsAGC
NM_001291317.2:c.493+1504_493+1506delinsAGC	NP_001278246.1:n.493+1504_493+1506delinsAGC
NM_001369493.1:c.763+1504_763+1506delinsAGC	NP_001356422.1:n.763+1504_763+1506delinsAGC