Canonical Allele Identifier: CA10603416

Gene: KCTD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.26501139G>A , CM000680.2:g.26501139G>A	GRCh38
NC_000018.9:g.24081103G>A , CM000680.1:g.24081103G>A	GRCh37
NC_000018.8:g.22335101G>A	NCBI36
NG_054919.1:g.161374C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580059.7:c.1921C>T MANE Select	ENSP00000463041.2:p.His641Tyr
ENST00000317932.11:c.97C>T	ENSP00000314831.7:p.His33Tyr
ENST00000408011.7:c.97C>T	ENSP00000384367.3:p.His33Tyr
ENST00000417602.5:c.97C>T	ENSP00000408405.2:p.His33Tyr
ENST00000578973.1:c.97C>T	ENSP00000463608.1:p.His33Tyr
ENST00000579973.5:c.97C>T	ENSP00000464170.1:p.His33Tyr
ENST00000580059.5:c.97C>T	ENSP00000463041.1:p.His33Tyr
ENST00000580191.5:c.121C>T	ENSP00000464261.1:p.His41Tyr
ENST00000580638.5:c.97C>T	ENSP00000462470.1:p.His33Tyr
NM_001136205.2:c.97C>T	NP_001129677.1:p.His33Tyr
NM_001142730.2:c.1921C>T	NP_001136202.1:p.His641Tyr
NM_001258221.1:c.97C>T	NP_001245150.1:p.His33Tyr
NM_001258222.1:c.121C>T	NP_001245151.1:p.His41Tyr
NM_198991.3:c.97C>T	NP_945342.1:p.His33Tyr
NM_001258222.2:c.121C>T	NP_001245151.1:p.His41Tyr
NM_001351443.1:c.97C>T	NP_001338372.1:p.His33Tyr
XR_002958168.1:n.2269C>T
NM_001142730.3:c.1921C>T MANE Select	NP_001136202.1:p.His641Tyr
NM_001258222.3:c.121C>T	NP_001245151.1:p.His41Tyr
NM_001258221.2:c.97C>T	NP_001245150.1:p.His33Tyr
NM_198991.4:c.97C>T	NP_945342.1:p.His33Tyr