Canonical Allele Identifier: CA359381373

Gene: AMACR C1QTNF3-AMACR

Linked Data

• gnomAD v4: 5-33998702-T-C
• MyVariant Identifiers: chr5:g.33998807T>C (hg19) ; chr5:g.33998702T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33998702T>C , CM000667.2:g.33998702T>C	GRCh38
NC_000005.9:g.33998807T>C , CM000667.1:g.33998807T>C	GRCh37
NC_000005.8:g.34034564T>C	NCBI36
NG_016211.1:g.14414A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335606.11:c.678A>G (AMACR) MANE Select	ENSP00000334424.6:p.Ala226=
ENST00000335606.10:c.678A>G (AMACR)	ENSP00000334424.6:p.Ala226=
ENST00000382068.3:c.517A>G (AMACR)	ENSP00000477108.1:p.Arg173Gly
ENST00000382072.6:c.517A>G (AMACR)	ENSP00000371504.2:p.Arg173Gly
ENST00000382079.3:c.*104A>G (C1QTNF3-AMACR)	ENSP00000371511.3:n.*104A>G
ENST00000382085.7:c.678A>G (AMACR)	ENSP00000371517.3:p.Ala226=
ENST00000426255.6:c.678A>G (AMACR)	ENSP00000476965.1:p.Ala226=
ENST00000502637.5:c.633A>G (AMACR)	ENSP00000424351.1:p.Ala211=
ENST00000506639.5:c.517A>G (AMACR)	ENSP00000427227.1:p.Arg173Gly
ENST00000512079.5:c.678A>G (AMACR)	ENSP00000477411.1:p.Ala226=
ENST00000514195.1:n.529A>G (AMACR)
NM_001167595.1:c.678A>G (AMACR)	NP_001161067.1:p.Ala226=
NM_014324.5:c.678A>G (AMACR)	NP_055139.4:p.Ala226=
NM_203382.2:c.517A>G (AMACR)	NP_976316.1:p.Arg173Gly
NR_037951.1:n.1034A>G (C1QTNF3-AMACR)
NM_014324.6:c.678A>G (AMACR) MANE Select	NP_055139.4:p.Ala226=
NM_001167595.2:c.678A>G (AMACR)	NP_001161067.1:p.Ala226=
NM_203382.3:c.517A>G (AMACR)	NP_976316.1:p.Arg173Gly