Linked Data
dbSNP Id:
rs748102555
ExAC:
21:38308771 C / CTGG
gnomAD v2:
21-38308771-C-CTGG
gnomAD v3:
21-36936471-C-CTGG
gnomAD v4:
21-36936471-C-CTGG
MyVariant Identifiers:
chr21:g.38308771_38308772insTGG (hg19)
chr21:g.36936471_36936472insTGG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.36936471_36936472insTGG , CM000683.2:g.36936471_36936472insTGG | GRCh38 |
| NC_000021.8:g.38308771_38308772insTGG , CM000683.1:g.38308771_38308772insTGG | GRCh37 |
| NC_000021.7:g.37230641_37230642insTGG | NCBI36 |
| NG_016193.1:g.58765_58766insCCA | |
| NG_016193.2:g.58923_58924insCCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000674895.3:c.1414_1415insCCA MANE Select | ENSP00000502087.2:p.Gly472delinsAlaArg | |
| ENST00000674895.2:c.973_974insCCA | ENSP00000502087.1:p.Gly325delinsAlaArg | |
| ENST00000675057.1:c.973_974insCCA | ENSP00000501832.1:p.Gly325delinsAlaArg | |
| ENST00000675307.1:c.973_974insCCA | ENSP00000501750.1:p.Gly325delinsAlaArg | |
| ENST00000336648.8:c.973_974insCCA | ENSP00000338387.3:p.Gly325delinsAlaArg | |
| ENST00000399120.5:c.973_974insCCA | ENSP00000382071.1:p.Gly325delinsAlaArg | |
| ENST00000612277.4:c.973_974insCCA | ENSP00000479939.1:p.Gly325delinsAlaArg | |
| NM_000411.6:c.973_974insCCA | NP_000402.3:p.Gly325delinsAlaArg | |
| NM_001242784.1:c.973_974insCCA | NP_001229713.1:p.Gly325delinsAlaArg | |
| NM_001242785.1:c.973_974insCCA | NP_001229714.1:p.Gly325delinsAlaArg | |
| XM_005260953.2:c.1414_1415insCCA | XP_005261010.1:p.Gly472delinsAlaArg | |
| XM_005260954.1:c.1414_1415insCCA | XP_005261011.1:p.Gly472delinsAlaArg | |
| XM_005260955.2:c.973_974insCCA | XP_005261012.1:p.Gly325delinsAlaArg | |
| XM_005260956.2:c.973_974insCCA | XP_005261013.1:p.Gly325delinsAlaArg | |
| XM_006723994.1:c.973_974insCCA | XP_006724057.1:p.Gly325delinsAlaArg | |
| XM_006723995.1:c.973_974insCCA | XP_006724058.1:p.Gly325delinsAlaArg | |
| XM_011529538.1:c.973_974insCCA | XP_011527840.1:p.Gly325delinsAlaArg | |
| XM_011529539.1:c.973_974insCCA | XP_011527841.1:p.Gly325delinsAlaArg | |
| XM_011529540.1:c.1414_1415insCCA | XP_011527842.1:p.Gly472delinsAlaArg | |
| XM_011529541.1:c.973_974insCCA | XP_011527843.1:p.Gly325delinsAlaArg | |
| XM_011529542.1:c.1414_1415insCCA | XP_011527844.1:p.Gly472delinsAlaArg | |
| NM_000411.7:c.973_974insCCA | NP_000402.3:p.Gly325delinsAlaArg | |
| NM_001242784.2:c.973_974insCCA | NP_001229713.1:p.Gly325delinsAlaArg | |
| NM_001242785.2:c.973_974insCCA | NP_001229714.1:p.Gly325delinsAlaArg | |
| NM_001352514.1:c.1414_1415insCCA | NP_001339443.1:p.Gly472delinsAlaArg | |
| NM_001352515.1:c.973_974insCCA | NP_001339444.1:p.Gly325delinsAlaArg | |
| NM_001352516.1:c.973_974insCCA | NP_001339445.1:p.Gly325delinsAlaArg | |
| NM_001352517.1:c.973_974insCCA | NP_001339446.1:p.Gly325delinsAlaArg | |
| NM_001352518.1:c.973_974insCCA | NP_001339447.1:p.Gly325delinsAlaArg | |
| NR_148020.1:n.1456_1457insCCA | ||
| NR_148021.1:n.1430_1431insCCA | ||
| XM_011529539.3:c.973_974insCCA | XP_011527841.1:p.Gly325delinsAlaArg | |
| XM_011529540.2:c.1414_1415insCCA | XP_011527842.1:p.Gly472delinsAlaArg | |
| XM_017028330.1:c.973_974insCCA | XP_016883819.1:p.Gly325delinsAlaArg | |
| XM_024452065.1:c.802_803insCCA | XP_024307833.1:p.Gly268delinsAlaArg | |
| XM_024452066.1:c.802_803insCCA | XP_024307834.1:p.Gly268delinsAlaArg | |
| XR_001754835.1:n.1415_1416insCCA | ||
| XR_001754836.1:n.1415_1416insCCA | ||
| XR_001754837.2:n.1415_1416insCCA | ||
| XR_001754840.1:n.1415_1416insCCA | ||
| NM_000411.8:c.973_974insCCA | NP_000402.3:p.Gly325delinsAlaArg | |
| NM_001242784.3:c.973_974insCCA | NP_001229713.1:p.Gly325delinsAlaArg | |
| NM_001352514.2:c.1414_1415insCCA MANE Select | NP_001339443.1:p.Gly472delinsAlaArg | |
| NM_001352515.2:c.973_974insCCA | NP_001339444.1:p.Gly325delinsAlaArg | |
| NM_001352516.2:c.973_974insCCA | NP_001339445.1:p.Gly325delinsAlaArg | |
| NR_148020.2:n.1273_1274insCCA | ||
| NM_001352518.2:c.973_974insCCA | NP_001339447.1:p.Gly325delinsAlaArg |