Canonical Allele Identifier: CA1538228980

Gene: AMACR C1QTNF3-AMACR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33989413C= , CM000667.2:g.33989413C=	GRCh38
NC_000005.9:g.33989518C= , CM000667.1:g.33989518C=	GRCh37
NC_000005.8:g.34025275C=	NCBI36
NG_011691.2:g.263G=
NG_016211.1:g.23703G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335606.11:c.829G= (AMACR) MANE Select	ENSP00000334424.6:p.Glu277=
ENST00000335606.10:c.829G= (AMACR)	ENSP00000334424.6:p.Glu277=
ENST00000382072.6:c.*71G= (AMACR)	ENSP00000371504.2:n.*71G=
ENST00000382079.3:c.*255G= (C1QTNF3-AMACR)	ENSP00000371511.3:n.*255G=
ENST00000382085.7:c.829G= (AMACR)	ENSP00000371517.3:p.Glu277=
ENST00000502637.5:c.784G= (AMACR)	ENSP00000424351.1:p.Glu262=
ENST00000506639.5:c.*151G= (AMACR)	ENSP00000427227.1:n.*151G=
ENST00000514195.1:n.723G= (AMACR)
NM_001167595.1:c.829G= (AMACR)	NP_001161067.1:p.Glu277=
NM_014324.5:c.829G= (AMACR)	NP_055139.4:p.Glu277=
NM_203382.2:c.*71G= (AMACR)	NP_976316.1:n.*71G=
NR_037951.1:n.1185G= (C1QTNF3-AMACR)
NM_014324.6:c.829G= (AMACR) MANE Select	NP_055139.4:p.Glu277=
NM_001167595.2:c.829G= (AMACR)	NP_001161067.1:p.Glu277=
NM_203382.3:c.*71G= (AMACR)	NP_976316.1:n.*71G=