Linked Data
dbSNP Id:
rs1567619567
gnomAD v2:
17-3401808-A-T
gnomAD v3:
17-3498514-A-T
gnomAD v4:
17-3498514-A-T
MyVariant Identifiers:
chr17:g.3401808_3401818delinsTTTTTTCGTAT (hg19)
chr17:g.3498514_3498524delinsTTTTTTCGTAT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.3498514A>T , CM000679.2:g.3498514A>T | GRCh38 |
| NC_000017.10:g.3401808A>T , CM000679.1:g.3401808A>T | GRCh37 |
| NC_000017.9:g.3348558A>T | NCBI36 |
| NG_008399.1:g.29405A>T | |
| NG_008399.2:g.29869A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263080.3:c.745-377A>T (ASPA) MANE Select | ENSP00000263080.2:n.745-377A>T | |
| ENST00000263080.2:c.745-377A>T (ASPA) | ENSP00000263080.2:n.745-377A>T | |
| ENST00000456349.6:c.745-377A>T (ASPA) | ENSP00000409976.2:n.745-377A>T | |
| ENST00000541913.5:c.-74+14898T>A (SPATA22) | ENSP00000441920.1:n.-74+14898T>A | |
| ENST00000570318.1:c.-74+15097T>A (SPATA22) | ENSP00000459147.1:n.-74+15097T>A | |
| NM_000049.2:c.745-377A>T (ASPA) | NP_000040.1:n.745-377A>T | |
| NM_001128085.1:c.745-377A>T (ASPA) | NP_001121557.1:n.745-377A>T | |
| XM_005256829.1:c.-74+14898T>A (SPATA22) | XP_005256886.1:n.-74+14898T>A | |
| XM_005256830.1:c.-74+14898T>A (SPATA22) | XP_005256887.1:n.-74+14898T>A | |
| XM_006721527.2:c.745-377A>T (ASPA) | XP_006721590.1:n.745-377A>T | |
| XR_934026.1:n.1012-377A>T (ASPA) | ||
| NM_001321336.1:c.-74+14898T>A (SPATA22) | NP_001308265.1:n.-74+14898T>A | |
| NM_001321337.1:c.-74+14898T>A (SPATA22) | NP_001308266.1:n.-74+14898T>A | |
| XM_017024661.1:c.745-377A>T (ASPA) | XP_016880150.1:n.745-377A>T | |
| XM_024450764.1:c.745-377A>T (ASPA) | XP_024306532.1:n.745-377A>T | |
| XR_934026.2:n.1012-377A>T (ASPA) | ||
| NM_000049.3:c.745-377A>T (ASPA) | NP_000040.1:n.745-377A>T | |
| NM_000049.4:c.745-377A>T (ASPA) MANE Select | NP_000040.1:n.745-377A>T | |
| NM_001321336.2:c.-74+14898T>A (SPATA22) | NP_001308265.1:n.-74+14898T>A | |
| NM_001321337.2:c.-74+14898T>A (SPATA22) | NP_001308266.1:n.-74+14898T>A |