Canonical Allele Identifier: CA14619673

Gene: KCTD1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.26576461G>T , CM000680.2:g.26576461G>T	GRCh38
NC_000018.9:g.24156425G>T , CM000680.1:g.24156425G>T	GRCh37
NC_000018.8:g.22410423G>T	NCBI36
NG_054919.1:g.86052C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317932.11:c.-16+52686C>A	ENSP00000314831.7:n.-16+52686C>A
ENST00000579973.5:c.-16+52686C>A	ENSP00000464170.1:n.-16+52686C>A
ENST00000580191.5:c.10-75211C>A	ENSP00000464261.1:n.10-75211C>A
NM_001258222.1:c.10-75211C>A	NP_001245151.1:n.10-75211C>A
NM_198991.3:c.-16+52686C>A	NP_945342.1:n.-16+52686C>A
NM_001258222.2:c.10-75211C>A	NP_001245151.1:n.10-75211C>A
NM_001258222.3:c.10-75211C>A	NP_001245151.1:n.10-75211C>A
NM_198991.4:c.-16+52686C>A	NP_945342.1:n.-16+52686C>A