Canonical Allele Identifier: CA13632129
Gene: KCTD10 HGNC NCBI

Linked Data

dbSNP Id: rs2338104
gnomAD v2: 12-109895168-C-G
gnomAD v3: 12-109457363-C-G
gnomAD v4: 12-109457363-C-G
MyVariant Identifiers: chr12:g.109895168C>G (hg19) chr12:g.109457363C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109457363C>G , CM000674.2:g.109457363C>G GRCh38
NC_000012.11:g.109895168C>G , CM000674.1:g.109895168C>G GRCh37
NC_000012.10:g.108379551C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000228495.11:c.527+267G>C MANE Select ENSP00000228495.6:n.527+267G>C
ENST00000228495.10:c.527+267G>C ENSP00000228495.6:n.527+267G>C
ENST00000440541.6:c.*123+267G>C ENSP00000390321.2:n.*123+267G>C
ENST00000535546.5:c.-17+267G>C ENSP00000441586.1:n.-17+267G>C
ENST00000537165.5:c.*1984+267G>C ENSP00000474497.1:n.*1984+267G>C
ENST00000538161.5:n.424+267G>C
ENST00000540089.5:c.-17+267G>C ENSP00000439722.1:n.-17+267G>C
ENST00000540355.5:c.-17+267G>C ENSP00000440008.1:n.-17+267G>C
ENST00000540402.1:n.346+267G>C
ENST00000540411.5:c.518+267G>C ENSP00000441672.1:n.518+267G>C
ENST00000541077.1:c.*305+267G>C ENSP00000474870.1:n.*305+267G>C
ENST00000542262.5:c.440+267G>C ENSP00000437348.1:n.440+267G>C
ENST00000542858.1:c.497+267G>C ENSP00000445129.1:n.497+267G>C
ENST00000542954.5:c.-17+267G>C ENSP00000439481.1:n.-17+267G>C
ENST00000545759.5:n.2267G>C
NM_031954.3:c.527+267G>C NP_114160.1:n.527+267G>C
XM_005253946.2:c.530+267G>C XP_005254003.1:n.530+267G>C
XM_011538795.1:c.530+267G>C XP_011537097.1:n.530+267G>C
NM_001317395.1:c.530+267G>C NP_001304324.1:n.530+267G>C
NM_001317399.1:c.527+267G>C NP_001304328.1:n.527+267G>C
NM_031954.4:c.527+267G>C NP_114160.1:n.527+267G>C
NR_133897.1:n.639+267G>C
NR_133898.1:n.595+267G>C
NM_031954.5:c.527+267G>C MANE Select NP_114160.1:n.527+267G>C
NM_001317395.2:c.530+267G>C NP_001304324.1:n.530+267G>C
NM_001317399.2:c.527+267G>C NP_001304328.1:n.527+267G>C
NR_133897.2:n.395+267G>C
NR_133898.2:n.351+267G>C
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