Linked Data
ClinVar Variation Id:
725410
ClinVar RCV Id:
RCV002068636
dbSNP Id:
rs778140879
ExAC:
5:33998804 A / G
gnomAD v2:
5-33998804-A-G
gnomAD v3:
5-33998699-A-G
gnomAD v4:
5-33998699-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.33998699A>G , CM000667.2:g.33998699A>G | GRCh38 |
| NC_000005.9:g.33998804A>G , CM000667.1:g.33998804A>G | GRCh37 |
| NC_000005.8:g.34034561A>G | NCBI36 |
| NG_016211.1:g.14417T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000335606.11:c.681T>C (AMACR) MANE Select | ENSP00000334424.6:p.Asp227= | |
| ENST00000335606.10:c.681T>C (AMACR) | ENSP00000334424.6:p.Asp227= | |
| ENST00000382068.3:c.520T>C (AMACR) | ENSP00000477108.1:p.Trp174Arg | |
| ENST00000382072.6:c.520T>C (AMACR) | ENSP00000371504.2:p.Trp174Arg | |
| ENST00000382079.3:c.*107T>C (C1QTNF3-AMACR) | ENSP00000371511.3:n.*107T>C | |
| ENST00000382085.7:c.681T>C (AMACR) | ENSP00000371517.3:p.Asp227= | |
| ENST00000426255.6:c.681T>C (AMACR) | ENSP00000476965.1:p.Asp227= | |
| ENST00000502637.5:c.636T>C (AMACR) | ENSP00000424351.1:p.Asp212= | |
| ENST00000506639.5:c.520T>C (AMACR) | ENSP00000427227.1:p.Trp174Arg | |
| ENST00000512079.5:c.681T>C (AMACR) | ENSP00000477411.1:p.Asp227= | |
| ENST00000514195.1:n.532T>C (AMACR) | ||
| NM_001167595.1:c.681T>C (AMACR) | NP_001161067.1:p.Asp227= | |
| NM_014324.5:c.681T>C (AMACR) | NP_055139.4:p.Asp227= | |
| NM_203382.2:c.520T>C (AMACR) | NP_976316.1:p.Trp174Arg | |
| NR_037951.1:n.1037T>C (C1QTNF3-AMACR) | ||
| NM_014324.6:c.681T>C (AMACR) MANE Select | NP_055139.4:p.Asp227= | |
| NM_001167595.2:c.681T>C (AMACR) | NP_001161067.1:p.Asp227= | |
| NM_203382.3:c.520T>C (AMACR) | NP_976316.1:p.Trp174Arg |