Canonical Allele Identifier: CA2673481316

Gene: AMACR C1QTNF3-AMACR

Linked Data

• gnomAD v4: 5-33998592-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33998592A>G , CM000667.2:g.33998592A>G	GRCh38
NC_000005.9:g.33998697A>G , CM000667.1:g.33998697A>G	GRCh37
NC_000005.8:g.34034454A>G	NCBI36
NG_016211.1:g.14524T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000335606.11:c.739+49T>C (AMACR) MANE Select	ENSP00000334424.6:n.739+49T>C
ENST00000335606.10:c.739+49T>C (AMACR)	ENSP00000334424.6:n.739+49T>C
ENST00000382068.3:c.578+49T>C (AMACR)	ENSP00000477108.1:n.578+49T>C
ENST00000382072.6:c.578+49T>C (AMACR)	ENSP00000371504.2:n.578+49T>C
ENST00000382079.3:c.*165+49T>C (C1QTNF3-AMACR)	ENSP00000371511.3:n.*165+49T>C
ENST00000382085.7:c.739+49T>C (AMACR)	ENSP00000371517.3:n.739+49T>C
ENST00000426255.6:c.739+49T>C (AMACR)	ENSP00000476965.1:n.739+49T>C
ENST00000502637.5:c.694+49T>C (AMACR)	ENSP00000424351.1:n.694+49T>C
ENST00000506639.5:c.578+49T>C (AMACR)	ENSP00000427227.1:n.578+49T>C
ENST00000512079.5:c.739+49T>C (AMACR)	ENSP00000477411.1:n.739+49T>C
ENST00000514195.1:n.590+49T>C (AMACR)
NM_001167595.1:c.739+49T>C (AMACR)	NP_001161067.1:n.739+49T>C
NM_014324.5:c.739+49T>C (AMACR)	NP_055139.4:n.739+49T>C
NM_203382.2:c.578+49T>C (AMACR)	NP_976316.1:n.578+49T>C
NR_037951.1:n.1095+49T>C (C1QTNF3-AMACR)
NM_014324.6:c.739+49T>C (AMACR) MANE Select	NP_055139.4:n.739+49T>C
NM_001167595.2:c.739+49T>C (AMACR)	NP_001161067.1:n.739+49T>C
NM_203382.3:c.578+49T>C (AMACR)	NP_976316.1:n.578+49T>C