Canonical Allele Identifier: CA1538240454

Gene: AMACR C1QTNF3-AMACR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33998707T= , CM000667.2:g.33998707T=	GRCh38
NC_000005.9:g.33998812T= , CM000667.1:g.33998812T=	GRCh37
NC_000005.8:g.34034569T=	NCBI36
NG_016211.1:g.14409A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335606.11:c.673A= (AMACR) MANE Select	ENSP00000334424.6:p.Thr225=
ENST00000335606.10:c.673A= (AMACR)	ENSP00000334424.6:p.Thr225=
ENST00000382068.3:c.512A= (AMACR)	ENSP00000477108.1:p.Asp171=
ENST00000382072.6:c.512A= (AMACR)	ENSP00000371504.2:p.Asp171=
ENST00000382079.3:c.*99A= (C1QTNF3-AMACR)	ENSP00000371511.3:n.*99A=
ENST00000382085.7:c.673A= (AMACR)	ENSP00000371517.3:p.Thr225=
ENST00000426255.6:c.673A= (AMACR)	ENSP00000476965.1:p.Thr225=
ENST00000502637.5:c.628A= (AMACR)	ENSP00000424351.1:p.Thr210=
ENST00000506639.5:c.512A= (AMACR)	ENSP00000427227.1:p.Asp171=
ENST00000512079.5:c.673A= (AMACR)	ENSP00000477411.1:p.Thr225=
ENST00000514195.1:n.524A= (AMACR)
NM_001167595.1:c.673A= (AMACR)	NP_001161067.1:p.Thr225=
NM_014324.5:c.673A= (AMACR)	NP_055139.4:p.Thr225=
NM_203382.2:c.512A= (AMACR)	NP_976316.1:p.Asp171=
NR_037951.1:n.1029A= (C1QTNF3-AMACR)
NM_014324.6:c.673A= (AMACR) MANE Select	NP_055139.4:p.Thr225=
NM_001167595.2:c.673A= (AMACR)	NP_001161067.1:p.Thr225=
NM_203382.3:c.512A= (AMACR)	NP_976316.1:p.Asp171=