Linked Data
gnomAD v2:
12-52314707-CA-C
gnomAD v4:
12-51920923-CA-C
MyVariant Identifiers:
chr12:g.52314708del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.51920924del , CM000674.2:g.51920924del | GRCh38 |
| NC_000012.11:g.52314708del , CM000674.1:g.52314708del | GRCh37 |
| NC_000012.10:g.50600975del | NCBI36 |
| NG_009549.1:g.18507del , LRG_543:g.18507del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000551576.6:c.*31del | ENSP00000455848.2:n.*31del | |
| ENST00000388922.9:c.*31del MANE Select | ENSP00000373574.4:n.*31del | |
| ENST00000388922.8:c.*31del | ENSP00000373574.4:n.*31del | |
| ENST00000419526.6:c.*31del | ENSP00000392492.2:n.*31del | |
| ENST00000550683.5:c.*31del | ENSP00000447884.1:n.*31del | |
| NM_000020.2:c.*31del , LRG_543t1:c.*31del | NP_000011.2:n.*31del | |
| NM_001077401.1:c.*31del | NP_001070869.1:n.*31del | |
| XM_005269235.2:c.*31del | XP_005269292.1:n.*31del | |
| XM_011539008.1:c.*31del | XP_011537310.1:n.*31del | |
| XM_024449279.1:c.*31del | XP_024305047.1:n.*31del | |
| NM_000020.3:c.*31del MANE Select | NP_000011.2:n.*31del | |
| NM_001077401.2:c.*31del | NP_001070869.1:n.*31del |