Canonical Allele Identifier: CA13332983
Gene: DUSP29 HGNC NCBI

Linked Data

dbSNP Id: rs7919006
gnomAD v2: 10-76808760-C-T
gnomAD v3: 10-75049002-C-T
gnomAD v4: 10-75049002-C-T
MyVariant Identifiers: chr10:g.76808760C>T (hg19) chr10:g.75049002C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.75049002C>T , CM000672.2:g.75049002C>T GRCh38
NC_000010.10:g.76808760C>T , CM000672.1:g.76808760C>T GRCh37
NC_000010.9:g.76478766C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000338487.6:c.201-4985G>A MANE Select ENSP00000340609.5:n.201-4985G>A
ENST00000338487.5:c.201-4985G>A ENSP00000340609.5:n.201-4985G>A
NM_001003892.1:c.201-4985G>A NP_001003892.1:n.201-4985G>A
XM_005269762.2:c.201-4985G>A XP_005269819.1:n.201-4985G>A
XM_011539747.1:c.201-4985G>A XP_011538049.1:n.201-4985G>A
NM_001003892.2:c.201-4985G>A NP_001003892.1:n.201-4985G>A
XM_011539747.2:c.201-4985G>A XP_011538049.1:n.201-4985G>A
XM_017016176.1:c.201-4180G>A XP_016871665.1:n.201-4180G>A
NM_001003892.3:c.201-4985G>A MANE Select NP_001003892.1:n.201-4985G>A
NM_001384909.1:c.201-4985G>A NP_001371838.1:n.201-4985G>A
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