Linked Data
gnomAD v3:
4-78911355-A-G
gnomAD v4:
4-78911355-A-G
MyVariant Identifiers:
chr4:g.79832509A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.78911355A>G , CM000666.2:g.78911355A>G | GRCh38 |
| NC_000004.11:g.79832509A>G , CM000666.1:g.79832509A>G | GRCh37 |
| NC_000004.10:g.80051533A>G | NCBI36 |
| NG_047162.1:g.139978A>G | |
| NG_053104.1:g.33084T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502613.3:c.2808A>G (BMP2K) MANE Select | ENSP00000424668.2:p.Pro936= | |
| ENST00000335016.9:c.2808A>G (BMP2K) | ENSP00000334836.5:p.Pro936= | |
| ENST00000342820.10:c.*782+3855T>C (PAQR3) | ENSP00000344203.6:n.*782+3855T>C | |
| ENST00000502613.1:c.1885A>G (BMP2K) | ||
| ENST00000511594.5:c.*834T>C (PAQR3) | ENSP00000425080.1:n.*834T>C | |
| ENST00000512760.5:c.*792+3855T>C (PAQR3) | ENSP00000426875.1:n.*792+3855T>C | |
| ENST00000628286.1:c.*1784A>G (BMP2K) | ENSP00000487317.1:n.*1784A>G | |
| NM_198892.1:c.2808A>G (BMP2K) | NP_942595.1:p.Pro936= | |
| XM_005263117.1:c.2697A>G (BMP2K) | XP_005263174.1:p.Pro899= | |
| XM_011532101.1:c.2568A>G (BMP2K) | XP_011530403.1:p.Pro856= | |
| XR_938694.1:n.1118-5194T>C (PAQR3) | ||
| XM_017008381.1:c.2568A>G (BMP2K) | XP_016863870.1:p.Pro856= | |
| XM_017008382.1:c.1920A>G (BMP2K) | XP_016863871.1:p.Pro640= | |
| XR_938694.3:n.1098-5194T>C (PAQR3) | ||
| NM_198892.2:c.2808A>G (BMP2K) MANE Select | NP_942595.1:p.Pro936= |