Canonical Allele Identifier: CA359381378

Gene: AMACR C1QTNF3-AMACR

Linked Data

• MyVariant Identifiers: chr5:g.33998808G>T (hg19) ; chr5:g.33998703G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33998703G>T , CM000667.2:g.33998703G>T	GRCh38
NC_000005.9:g.33998808G>T , CM000667.1:g.33998808G>T	GRCh37
NC_000005.8:g.34034565G>T	NCBI36
NG_016211.1:g.14413C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335606.11:c.677C>A (AMACR) MANE Select	ENSP00000334424.6:p.Ala226Glu
ENST00000335606.10:c.677C>A (AMACR)	ENSP00000334424.6:p.Ala226Glu
ENST00000382068.3:c.516C>A (AMACR)	ENSP00000477108.1:p.Ser172Arg
ENST00000382072.6:c.516C>A (AMACR)	ENSP00000371504.2:p.Ser172Arg
ENST00000382079.3:c.*103C>A (C1QTNF3-AMACR)	ENSP00000371511.3:n.*103C>A
ENST00000382085.7:c.677C>A (AMACR)	ENSP00000371517.3:p.Ala226Glu
ENST00000426255.6:c.677C>A (AMACR)	ENSP00000476965.1:p.Ala226Glu
ENST00000502637.5:c.632C>A (AMACR)	ENSP00000424351.1:p.Ala211Glu
ENST00000506639.5:c.516C>A (AMACR)	ENSP00000427227.1:p.Ser172Arg
ENST00000512079.5:c.677C>A (AMACR)	ENSP00000477411.1:p.Ala226Glu
ENST00000514195.1:n.528C>A (AMACR)
NM_001167595.1:c.677C>A (AMACR)	NP_001161067.1:p.Ala226Glu
NM_014324.5:c.677C>A (AMACR)	NP_055139.4:p.Ala226Glu
NM_203382.2:c.516C>A (AMACR)	NP_976316.1:p.Ser172Arg
NR_037951.1:n.1033C>A (C1QTNF3-AMACR)
NM_014324.6:c.677C>A (AMACR) MANE Select	NP_055139.4:p.Ala226Glu
NM_001167595.2:c.677C>A (AMACR)	NP_001161067.1:p.Ala226Glu
NM_203382.3:c.516C>A (AMACR)	NP_976316.1:p.Ser172Arg