Linked Data
dbSNP Id:
rs782414344
ExAC:
X:152959675 C / T
gnomAD v2:
X-152959675-C-T
gnomAD v4:
X-153694220-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153694220C>T , CM000685.2:g.153694220C>T | GRCh38 |
| NC_000023.10:g.152959675C>T , CM000685.1:g.152959675C>T | GRCh37 |
| NC_000023.9:g.152612869C>T | NCBI36 |
| NG_012016.1:g.10924C>T | |
| NG_012016.2:g.10924C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253122.10:c.1345C>T MANE Select | ENSP00000253122.5:p.Leu449Phe | |
| ENST00000253122.9:c.1345C>T | ENSP00000253122.5:p.Leu449Phe | |
| ENST00000413787.1:c.274C>T | ENSP00000400463.1:p.Leu92Phe | |
| ENST00000430077.6:c.1000C>T | ENSP00000403041.2:p.Leu334Phe | |
| ENST00000442457.1:c.399C>T | ||
| ENST00000485324.1:n.1490C>T | ||
| NM_001142805.1:c.1315C>T | NP_001136277.1:p.Leu439Phe | |
| NM_001142806.1:c.1000C>T | NP_001136278.1:p.Leu334Phe | |
| NM_005629.3:c.1345C>T | NP_005620.1:p.Leu449Phe | |
| NM_005629.4:c.1345C>T MANE Select | NP_005620.1:p.Leu449Phe | |
| NM_001142805.2:c.1315C>T | NP_001136277.1:p.Leu439Phe |