Linked Data
gnomAD v3:
X-111401272-A-G
gnomAD v4:
X-111401272-A-G
MyVariant Identifiers:
chrX:g.110644500A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.111401272A>G , CM000685.2:g.111401272A>G | GRCh38 |
| NC_000023.10:g.110644500A>G , CM000685.1:g.110644500A>G | GRCh37 |
| NC_000023.9:g.110531156A>G | NCBI36 |
| NG_011750.1:g.15907T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356220.8:c.423T>C | ENSP00000348553.4:p.Asn141= | |
| ENST00000358070.10:c.423T>C | ENSP00000350776.5:p.Asn141= | |
| ENST00000371993.7:c.423T>C | ENSP00000361061.3:p.Asn141= | |
| ENST00000468911.2:c.423T>C | ENSP00000418811.2:p.Asn141= | |
| ENST00000488120.2:c.423T>C | ENSP00000419861.1:p.Asn141= | |
| ENST00000496551.2:c.423T>C | ENSP00000490448.1:p.Asn141= | |
| ENST00000635795.1:c.423T>C | ENSP00000489635.1:p.Asn141= | |
| ENST00000636035.2:c.423T>C MANE Select | ENSP00000490614.1:p.Asn141= | |
| ENST00000636381.2:c.423T>C | ENSP00000490068.2:p.Asn141= | |
| ENST00000637453.1:c.423T>C | ENSP00000490357.1:p.Asn141= | |
| ENST00000637570.1:c.423T>C | ENSP00000490878.1:p.Asn141= | |
| ENST00000680476.1:c.423T>C | ENSP00000505501.1:p.Asn141= | |
| ENST00000338081.7:c.666T>C | ENSP00000337697.3:p.Asn222= | |
| ENST00000356220.7:c.423T>C | ENSP00000348553.3:p.Asn141= | |
| ENST00000358070.8:c.641T>C | ||
| ENST00000371993.6:c.423T>C | ENSP00000361061.2:p.Asn141= | |
| ENST00000488120.1:c.423T>C | ENSP00000419861.1:p.Asn141= | |
| ENST00000496551.1:n.663T>C | ||
| NM_000555.3:c.666T>C | NP_000546.2:p.Asn222= | |
| NM_001195553.1:c.423T>C | NP_001182482.1:p.Asn141= | |
| NM_178151.2:c.423T>C | NP_835364.1:p.Asn141= | |
| NM_178152.2:c.423T>C | NP_835365.1:p.Asn141= | |
| NM_178153.2:c.423T>C | NP_835366.1:p.Asn141= | |
| XM_011530878.1:c.423T>C | XP_011529180.1:p.Asn141= | |
| XM_011530879.1:c.423T>C | XP_011529181.1:p.Asn141= | |
| XM_011530880.1:c.423T>C | XP_011529182.1:p.Asn141= | |
| XM_011530878.3:c.423T>C | XP_011529180.1:p.Asn141= | |
| XM_011530879.3:c.423T>C | XP_011529181.1:p.Asn141= | |
| XM_011530880.3:c.423T>C | XP_011529182.1:p.Asn141= | |
| XM_017029312.2:c.423T>C | XP_016884801.1:p.Asn141= | |
| NM_001195553.2:c.423T>C MANE Select | NP_001182482.1:p.Asn141= | |
| NM_001369370.1:c.423T>C | NP_001356299.1:p.Asn141= | |
| NM_001369371.1:c.423T>C | NP_001356300.1:p.Asn141= | |
| NM_001369372.1:c.423T>C | NP_001356301.1:p.Asn141= | |
| NM_001369373.1:c.423T>C | NP_001356302.1:p.Asn141= | |
| NM_001369374.1:c.423T>C | NP_001356303.1:p.Asn141= | |
| NM_178152.3:c.423T>C | NP_835365.1:p.Asn141= | |
| NM_178153.3:c.423T>C | NP_835366.1:p.Asn141= | |
| NM_178151.3:c.423T>C | NP_835364.1:p.Asn141= |