Canonical Allele Identifier: CA2386632789

Gene: IFNAR1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33341645A= , CM000683.2:g.33341645A=	GRCh38
NC_000021.8:g.34713951A= , CM000683.1:g.34713951A=	GRCh37
NC_000021.7:g.33635821A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000442071.3:c.376+471A=	ENSP00000400161.3:n.376+471A=
ENST00000651609.2:c.*93+471A=	ENSP00000498594.1:n.*93+471A=
ENST00000652450.2:c.169+471A=	ENSP00000498654.1:n.169+471A=
ENST00000652513.2:c.376+471A=	ENSP00000498491.1:n.376+471A=
ENST00000652654.3:c.376+471A=	ENSP00000498666.1:n.376+471A=
ENST00000700045.1:n.503+471A=
ENST00000700046.1:c.201-1623A=	ENSP00000514762.1:n.201-1623A=
ENST00000700080.1:c.169+471A=	ENSP00000514785.1:n.169+471A=
ENST00000700084.1:c.-89-3601A=	ENSP00000514786.1:n.-89-3601A=
ENST00000700087.1:n.497+471A=
ENST00000700099.1:n.928A=
ENST00000700301.1:n.497+471A=
ENST00000703514.1:c.376+471A=	ENSP00000515347.1:n.376+471A=
ENST00000703515.1:c.376+471A=	ENSP00000515348.1:n.376+471A=
ENST00000703516.1:c.201-3601A=	ENSP00000515349.1:n.201-3601A=
ENST00000703556.1:c.376+471A=	ENSP00000515372.1:n.376+471A=
ENST00000703557.1:c.376+471A=	ENSP00000515373.1:n.376+471A=
ENST00000703561.1:c.376+471A=	ENSP00000515377.1:n.376+471A=
ENST00000703562.1:c.376+471A=	ENSP00000515378.1:n.376+471A=
ENST00000703563.1:c.376+471A=	ENSP00000515379.1:n.376+471A=
ENST00000703564.1:c.*93+471A=	ENSP00000515380.1:n.*93+471A=
ENST00000703565.1:c.376+471A=	ENSP00000515381.1:n.376+471A=
ENST00000703778.1:n.422+471A=
ENST00000703779.1:c.201-1623A=	ENSP00000515477.1:n.201-1623A=
ENST00000270139.8:c.376+471A= MANE Select	ENSP00000270139.3:n.376+471A=
ENST00000442071.2:c.376+471A=	ENSP00000400161.2:n.376+471A=
ENST00000651609.1:c.*93+471A=	ENSP00000498594.1:n.*93+471A=
ENST00000652450.1:c.169+471A=	ENSP00000498654.1:n.169+471A=
ENST00000652513.1:c.376+471A=	ENSP00000498491.1:n.376+471A=
ENST00000652601.1:c.376+471A=	ENSP00000498231.1:n.376+471A=
ENST00000652654.1:c.376+471A=	ENSP00000498666.1:n.376+471A=
ENST00000270139.7:c.376+471A=	ENSP00000270139.3:n.376+471A=
ENST00000442071.1:c.376+471A=	ENSP00000400161.1:n.376+471A=
NM_000629.2:c.376+471A=	NP_000620.2:n.376+471A=
XM_005260964.1:c.169+471A=	XP_005261021.1:n.169+471A=
XM_011529552.1:c.376+471A=	XP_011527854.1:n.376+471A=
XM_005260964.2:c.169+471A=	XP_005261021.1:n.169+471A=
XM_011529552.2:c.376+471A=	XP_011527854.1:n.376+471A=
NM_000629.3:c.376+471A= MANE Select	NP_000620.2:n.376+471A=
NM_001384498.1:c.376+471A=	NP_001371427.1:n.376+471A=
NM_001384499.1:c.376+471A=	NP_001371428.1:n.376+471A=
NM_001384500.1:c.-411+471A=	NP_001371429.1:n.-411+471A=
NM_001384501.1:c.376+471A=	NP_001371430.1:n.376+471A=
NM_001384502.1:c.-87+471A=	NP_001371431.1:n.-87+471A=
NM_001384503.1:c.376+471A=	NP_001371432.1:n.376+471A=
NM_001384504.1:c.169+471A=	NP_001371433.1:n.169+471A=