Canonical Allele Identifier: CA3226043

Gene: AMACR C1QTNF3-AMACR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33989519T>A , CM000667.2:g.33989519T>A	GRCh38
NC_000005.9:g.33989624T>A , CM000667.1:g.33989624T>A	GRCh37
NC_000005.8:g.34025381T>A	NCBI36
NG_011691.2:g.157A>T
NG_016211.1:g.23597A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014324.6:c.740-17A>T (AMACR) MANE Select	NP_055139.4:n.740-17A>T
ENST00000335606.11:c.740-17A>T (AMACR) MANE Select	ENSP00000334424.6:n.740-17A>T
NM_001167595.1:c.740-17A>T (AMACR)	NP_001161067.1:n.740-17A>T
NM_001167595.2:c.740-17A>T (AMACR)	NP_001161067.1:n.740-17A>T
NM_014324.5:c.740-17A>T (AMACR)	NP_055139.4:n.740-17A>T
NM_203382.2:c.579-17A>T (AMACR)	NP_976316.1:n.579-17A>T
NM_203382.3:c.579-17A>T (AMACR)	NP_976316.1:n.579-17A>T
NR_037951.1:n.1096-17A>T (C1QTNF3-AMACR)
ENST00000335606.10:c.740-17A>T (AMACR)	ENSP00000334424.6:n.740-17A>T
ENST00000382072.6:c.579-17A>T (AMACR)	ENSP00000371504.2:n.579-17A>T
ENST00000382079.3:c.*166-17A>T (C1QTNF3-AMACR)	ENSP00000371511.3:n.*166-17A>T
ENST00000382085.7:c.740-17A>T (AMACR)	ENSP00000371517.3:n.740-17A>T
ENST00000502637.5:c.695-17A>T (AMACR)	ENSP00000424351.1:n.695-17A>T
ENST00000506639.5:c.*62-17A>T (AMACR)	ENSP00000427227.1:n.*62-17A>T
ENST00000514195.1:n.634-17A>T (AMACR)