Canonical Allele Identifier: CA96470740
Gene: KCTD8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.44210148A>G , CM000666.2:g.44210148A>G GRCh38
NC_000004.11:g.44212165A>G , CM000666.1:g.44212165A>G GRCh37
NC_000004.10:g.43906922A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360029.4:c.962-34898T>C MANE Select ENSP00000353129.3:n.962-34898T>C
ENST00000360029.3:c.962-34898T>C ENSP00000353129.3:n.962-34898T>C
ENST00000515268.1:c.169-34898T>C
NM_198353.2:c.962-34898T>C NP_938167.1:n.962-34898T>C
XM_011513689.1:c.1079-34898T>C XP_011511991.1:n.1079-34898T>C
XM_011513690.1:c.1046-34898T>C XP_011511992.1:n.1046-34898T>C
XM_011513690.3:c.1046-34898T>C XP_011511992.1:n.1046-34898T>C
NM_198353.3:c.962-34898T>C MANE Select NP_938167.1:n.962-34898T>C
Search 100 bp 5'
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