Canonical Allele Identifier: CA13105482
Gene: DNAJA1 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.33025505G>A
GRCh37 chr9:g.33025503G>A
gnomAD v2:
9:33025503 G / A
gnomAD v3:
9:33025505 G / A
gnomAD v4:
chr9-33025505-G-A
Joint Max Group AF 0.21921986 (AMR)
Genomes Max Group AF 0.21921986 (AMR)
Exomes Max Group AF 0.30425041 (NFE)
dbSNP:
2297216
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.33025505G>A , CM000671.2:g.33025505G>A GRCh38
NC_000009.11:g.33025503G>A , CM000671.1:g.33025503G>A GRCh37
NC_000009.10:g.33015503G>A NCBI36
NG_012821.2:g.4627C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330899.5:c.-11+122G>A MANE Select ENSP00000369127.3:n.-11+122G>A
ENST00000330899.4:c.-11+122G>A ENSP00000369127.3:n.-11+122G>A
ENST00000495015.5:n.98+122G>A
NM_001314039.1:c.-304+122G>A NP_001300968.1:n.-304+122G>A
NM_001539.2:c.-11+122G>A NP_001530.1:n.-11+122G>A
NM_001539.3:c.-11+122G>A NP_001530.1:n.-11+122G>A
NM_001539.4:c.-11+122G>A MANE Select NP_001530.1:n.-11+122G>A
NM_001314039.2:c.-304+122G>A NP_001300968.1:n.-304+122G>A
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