Canonical Allele Identifier: CA116872901

Gene: AMACR C1QTNF3-AMACR

Linked Data

• ClinVar Variation Id: 2909130
• ClinVar RCV Id: RCV003615379
• dbSNP Id: rs998840712
• gnomAD v3: 5-34007981-G-C
• gnomAD v4: 5-34007981-G-C
• MyVariant Identifiers: chr5:g.34008086G>C (hg19) ; chr5:g.34007981G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34007981G>C , CM000667.2:g.34007981G>C	GRCh38
NC_000005.9:g.34008086G>C , CM000667.1:g.34008086G>C	GRCh37
NC_000005.8:g.34043843G>C	NCBI36
NG_016211.1:g.5135C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335606.11:c.39C>G (AMACR) MANE Select	ENSP00000334424.6:p.Gly13=
ENST00000335606.10:c.39C>G (AMACR)	ENSP00000334424.6:p.Gly13=
ENST00000382068.3:c.39C>G (AMACR)	ENSP00000477108.1:p.Gly13=
ENST00000382072.6:c.39C>G (AMACR)	ENSP00000371504.2:p.Gly13=
ENST00000382079.3:c.690-2082C>G (C1QTNF3-AMACR)	ENSP00000371511.3:n.690-2082C>G
ENST00000382085.7:c.39C>G (AMACR)	ENSP00000371517.3:p.Gly13=
ENST00000426255.6:c.39C>G (AMACR)	ENSP00000476965.1:p.Gly13=
ENST00000502637.5:c.39C>G (AMACR)	ENSP00000424351.1:p.Gly13=
ENST00000506639.5:c.39C>G (AMACR)	ENSP00000427227.1:p.Gly13=
ENST00000512079.5:c.39C>G (AMACR)	ENSP00000477411.1:p.Gly13=
ENST00000514195.1:n.51C>G (AMACR)
NM_001167595.1:c.39C>G (AMACR)	NP_001161067.1:p.Gly13=
NM_014324.5:c.39C>G (AMACR)	NP_055139.4:p.Gly13=
NM_203382.2:c.39C>G (AMACR)	NP_976316.1:p.Gly13=
NR_037951.1:n.765-2082C>G (C1QTNF3-AMACR)
NM_014324.6:c.39C>G (AMACR) MANE Select	NP_055139.4:p.Gly13=
NM_001167595.2:c.39C>G (AMACR)	NP_001161067.1:p.Gly13=
NM_203382.3:c.39C>G (AMACR)	NP_976316.1:p.Gly13=