Linked Data
dbSNP Id:
rs17689882
gnomAD v2:
17-43906828-G-A
gnomAD v3:
17-45829462-G-A
gnomAD v4:
17-45829462-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.45829462G>A , CM000679.2:g.45829462G>A | GRCh38 |
| NC_000017.10:g.43906828G>A , CM000679.1:g.43906828G>A | GRCh37 |
| NC_000017.9:g.41262609G>A | NCBI36 |
| NG_009902.1:g.50201G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000580876.6:c.-92+141G>A (CRHR1) | ENSP00000516345.1:n.-92+141G>A | |
| ENST00000580955.6:n.447+141G>A (CRHR1) | ||
| ENST00000705340.1:n.709+141G>A (CRHR1) | ||
| ENST00000705341.1:c.*111+141G>A (CRHR1) | ENSP00000516114.1:n.*111+141G>A | |
| ENST00000705342.1:n.332+141G>A (CRHR1) | ||
| ENST00000705343.1:n.43G>A (CRHR1) | ||
| ENST00000314537.10:c.434+141G>A (CRHR1) MANE Select | ENSP00000326060.6:n.434+141G>A | |
| ENST00000293493.11:c.435-99G>A (CRHR1) | ENSP00000293493.8:n.435-99G>A | |
| ENST00000314537.9:c.434+141G>A (CRHR1) | ENSP00000326060.5:n.434+141G>A | |
| ENST00000339069.9:c.131+141G>A (CRHR1) | ENSP00000340522.6:n.131+141G>A | |
| ENST00000347197.9:c.434+141G>A (CRHR1) | ENSP00000239167.7:n.434+141G>A | |
| ENST00000352855.9:c.314+141G>A (CRHR1) | ENSP00000344068.5:n.314+141G>A | |
| ENST00000398285.7:c.435-99G>A (CRHR1) | ENSP00000381333.3:n.435-99G>A | |
| ENST00000577353.5:c.434+141G>A (CRHR1) | ENSP00000462016.1:n.434+141G>A | |
| ENST00000580955.5:c.447+141G>A (CRHR1) | ||
| ENST00000582766.5:n.290+141G>A (CRHR1) | ||
| ENST00000583888.1:c.218+141G>A (CRHR1) | ENSP00000462553.1:n.218+141G>A | |
| ENST00000619154.4:c.228+141G>A (CRHR1) | ENSP00000484545.1:n.228+141G>A | |
| ENST00000634540.1:c.-92+141G>A (LINC02210-CRHR1) | ENSP00000488912.1:n.-92+141G>A | |
| NM_001145146.1:c.435-99G>A (CRHR1) | NP_001138618.1:n.435-99G>A | |
| NM_001145147.1:c.314+141G>A (CRHR1) | NP_001138619.1:n.314+141G>A | |
| NM_001145148.1:c.434+141G>A (CRHR1) | NP_001138620.1:n.434+141G>A | |
| NM_001256299.2:c.-92+141G>A (LINC02210-CRHR1) | NP_001243228.1:n.-92+141G>A | |
| NM_001303016.1:c.131+141G>A (LINC02210-CRHR1) | NP_001289945.1:n.131+141G>A | |
| NM_001303018.1:c.-92+141G>A (CRHR1) | NP_001289947.1:n.-92+141G>A | |
| NM_001303020.1:c.131+141G>A (CRHR1) | NP_001289949.1:n.131+141G>A | |
| NM_004382.4:c.434+141G>A (CRHR1) | NP_004373.2:n.434+141G>A | |
| NM_001145146.2:c.435-99G>A (CRHR1) | NP_001138618.1:n.435-99G>A | |
| NM_001145147.2:c.314+141G>A (CRHR1) | NP_001138619.1:n.314+141G>A | |
| NM_001145148.2:c.434+141G>A (CRHR1) | NP_001138620.1:n.434+141G>A | |
| NM_001256299.3:c.-92+141G>A (LINC02210-CRHR1) | NP_001243228.1:n.-92+141G>A | |
| NM_001303018.2:c.-92+141G>A (CRHR1) | NP_001289947.1:n.-92+141G>A | |
| NM_004382.5:c.434+141G>A (CRHR1) MANE Select | NP_004373.2:n.434+141G>A | |
| NM_001303020.2:c.131+141G>A (CRHR1) | NP_001289949.1:n.131+141G>A |