Canonical Allele Identifier: CA985487159

Gene: MILR1

Linked Data

• dbSNP Id: rs1485896062
• gnomAD v3: 17-64462381-C-G
• gnomAD v4: 17-64462381-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64462381C>G , CM000679.2:g.64462381C>G	GRCh38
NC_000017.9:g.59888959C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619286.5:c.763+1449C>G MANE Select	ENSP00000482801.1:n.763+1449C>G
ENST00000612535.4:c.493+1449C>G	ENSP00000477504.1:n.493+1449C>G
ENST00000615220.4:c.763+1449C>G	ENSP00000480749.1:n.763+1449C>G
ENST00000616498.4:c.478+1449C>G	ENSP00000481318.1:n.478+1449C>G
ENST00000619286.4:c.763+1449C>G	ENSP00000482801.1:n.763+1449C>G
NM_001085423.1:c.763+1449C>G	NP_001078892.1:n.763+1449C>G
NM_001291316.1:c.478+1449C>G	NP_001278245.1:n.478+1449C>G
NM_001291317.1:c.493+1449C>G	NP_001278246.1:n.493+1449C>G
XM_005276872.3:c.889+1449C>G	XP_005276929.1:n.889+1449C>G
XM_005276874.3:c.889+1449C>G	XP_005276931.1:n.889+1449C>G
XM_005276875.3:c.889+1449C>G	XP_005276932.1:n.889+1449C>G
XM_005276876.3:c.889+1449C>G	XP_005276933.1:n.889+1449C>G
XM_005276877.3:c.604+1449C>G	XP_005276934.1:n.604+1449C>G
XM_005276878.2:c.589+1449C>G	XP_005276935.1:n.589+1449C>G
XM_011524627.1:c.889+1449C>G	XP_011522929.1:n.889+1449C>G
XM_017024486.1:c.889+1449C>G	XP_016879975.1:n.889+1449C>G
XM_017024487.1:c.589+1449C>G	XP_016879976.1:n.589+1449C>G
XM_024450706.1:c.889+1449C>G	XP_024306474.1:n.889+1449C>G
XM_024450707.1:c.889+1449C>G	XP_024306475.1:n.889+1449C>G
XM_024450708.1:c.889+1449C>G	XP_024306476.1:n.889+1449C>G
XM_024450709.1:c.889+1449C>G	XP_024306477.1:n.889+1449C>G
XR_002957989.1:n.910+1449C>G
XR_002957990.1:n.910+1449C>G
NM_001085423.2:c.763+1449C>G MANE Select	NP_001078892.1:n.763+1449C>G
NM_001291316.2:c.478+1449C>G	NP_001278245.1:n.478+1449C>G
NM_001291317.2:c.493+1449C>G	NP_001278246.1:n.493+1449C>G
NM_001369493.1:c.763+1449C>G	NP_001356422.1:n.763+1449C>G