Canonical Allele Identifier: CA1139921798

Gene: ARNT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150836413C= , CM000663.2:g.150836413C=	GRCh38
NC_000001.10:g.150808889C= , CM000663.1:g.150808889C=	GRCh37
NC_000001.9:g.149075513C=	NCBI36
NG_028248.1:g.45356G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358595.10:c.567G= MANE Select	ENSP00000351407.5:p.Val189=
ENST00000354396.6:c.567G=	ENSP00000346372.2:p.Val189=
ENST00000358595.9:c.567G=	ENSP00000351407.5:p.Val189=
ENST00000468970.1:n.87G=
ENST00000471844.6:c.567G=	ENSP00000425899.1:p.Val189=
ENST00000505755.5:c.522G=	ENSP00000427571.1:p.Val174=
ENST00000515192.5:c.540G=	ENSP00000423851.1:p.Val180=
NM_001197325.1:c.522G=	NP_001184254.1:p.Val174=
NM_001286035.1:c.540G=	NP_001272964.1:p.Val180=
NM_001286036.1:c.567G=	NP_001272965.1:p.Val189=
NM_001668.3:c.567G=	NP_001659.1:p.Val189=
NM_178427.2:c.522G=	NP_848514.1:p.Val174=
XM_005245151.1:c.567G=	XP_005245208.1:p.Val189=
XM_005245153.1:c.567G=	XP_005245210.1:p.Val189=
XM_005245154.2:c.540G=	XP_005245211.1:p.Val180=
XM_005245157.1:c.567G=	XP_005245214.1:p.Val189=
XM_011509542.1:c.564G=	XP_011507844.1:p.Val188=
XM_011509543.1:c.564G=	XP_011507845.1:p.Val188=
XM_011509544.1:c.561G=	XP_011507846.1:p.Val187=
XM_011509545.1:c.519G=	XP_011507847.1:p.Val173=
XM_011509546.1:c.471G=	XP_011507848.1:p.Val157=
XM_011509547.1:c.519G=	XP_011507849.1:p.Val173=
NM_001350224.1:c.540G=	NP_001337153.1:p.Val180=
NM_001350225.1:c.564G=	NP_001337154.1:p.Val188=
NM_001350226.1:c.561G=	NP_001337155.1:p.Val187=
XM_005245151.2:c.567G=	XP_005245208.1:p.Val189=
XM_011509543.3:c.564G=	XP_011507845.1:p.Val188=
XM_011509545.3:c.519G=	XP_011507847.1:p.Val173=
XM_011509546.2:c.471G=	XP_011507848.1:p.Val157=
XM_011509547.2:c.519G=	XP_011507849.1:p.Val173=
XM_017001288.2:c.540G=	XP_016856777.1:p.Val180=
XM_017001289.1:c.540G=	XP_016856778.1:p.Val180=
XM_017001290.2:c.495G=	XP_016856779.1:p.Val165=
XM_017001291.1:c.495G=	XP_016856780.1:p.Val165=
XM_017001292.1:c.540G=	XP_016856781.1:p.Val180=
XM_017001293.1:c.495G=	XP_016856782.1:p.Val165=
XM_017001294.1:c.567G=	XP_016856783.1:p.Val189=
XM_017001295.1:c.567G=	XP_016856784.1:p.Val189=
XM_017001296.1:c.522G=	XP_016856785.1:p.Val174=
NM_001668.4:c.567G= MANE Select	NP_001659.1:p.Val189=
NM_001197325.2:c.522G=	NP_001184254.1:p.Val174=
NM_001286035.2:c.540G=	NP_001272964.1:p.Val180=
NM_001286036.2:c.567G=	NP_001272965.1:p.Val189=
NM_001350224.2:c.540G=	NP_001337153.1:p.Val180=
NM_001350225.2:c.564G=	NP_001337154.1:p.Val188=
NM_001350226.2:c.561G=	NP_001337155.1:p.Val187=
NM_178427.3:c.522G=	NP_848514.1:p.Val174=