Linked Data
gnomAD v3:
Y-12915630-G-A
gnomAD v4:
Y-12915630-G-A
MyVariant Identifiers:
chrY:g.15027542G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12915630G>A , CM000686.2:g.12915630G>A | GRCh38 |
| NC_000024.9:g.15027542G>A , CM000686.1:g.15027542G>A | GRCh37 |
| NC_000024.8:g.13536936G>A | NCBI36 |
| NG_012831.1:g.16524G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000336079.8:c.1020G>A MANE Select | ENSP00000336725.3:p.Lys340= | |
| ENST00000336079.7:c.1020G>A | ENSP00000336725.3:p.Lys340= | |
| ENST00000360160.8:c.1020G>A | ENSP00000353284.4:p.Lys340= | |
| ENST00000495478.1:n.135G>A | ||
| NM_001122665.2:c.1020G>A | NP_001116137.1:p.Lys340= | |
| NM_001302552.1:c.1011G>A | NP_001289481.1:p.Lys337= | |
| NM_004660.4:c.1020G>A | NP_004651.2:p.Lys340= | |
| XM_006724878.1:c.1020G>A | XP_006724941.1:p.Lys340= | |
| XM_011531471.1:c.1020G>A | XP_011529773.1:p.Lys340= | |
| NM_001122665.3:c.1020G>A | NP_001116137.1:p.Lys340= | |
| NM_001302552.2:c.1011G>A | NP_001289481.1:p.Lys337= | |
| NM_001324195.1:c.1020G>A | NP_001311124.1:p.Lys340= | |
| NR_136716.1:n.1489G>A | ||
| NR_136717.1:n.1251G>A | ||
| NR_136718.1:n.1569G>A | ||
| NR_136719.1:n.1359G>A | ||
| NR_136720.1:n.1489G>A | ||
| NR_136721.1:n.1082G>A | ||
| NR_136722.1:n.1166G>A | ||
| NR_136723.1:n.1484G>A | ||
| NR_136724.1:n.1404G>A | ||
| XR_001756014.2:n.1124G>A | ||
| NM_004660.5:c.1020G>A MANE Select | NP_004651.2:p.Lys340= | |
| NM_001302552.3:c.1011G>A | NP_001289481.1:p.Lys337= | |
| NM_001324195.2:c.1020G>A | NP_001311124.1:p.Lys340= | |
| NR_136716.2:n.1407G>A | ||
| NR_136717.2:n.1169G>A | ||
| NR_136718.2:n.1487G>A | ||
| NR_136719.2:n.1277G>A | ||
| NR_136720.2:n.1407G>A | ||
| NR_136721.2:n.1072G>A |