Canonical Allele Identifier: CA343795290

Gene: KIAA0040

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.175160555G>A , CM000663.2:g.175160555G>A	GRCh38
NC_000001.10:g.175129691G>A , CM000663.1:g.175129691G>A	GRCh37
NC_000001.9:g.173396314G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423313.6:c.*159C>T MANE Select	ENSP00000462172.1:n.*159C>T
ENST00000423313.5:c.*159C>T	ENSP00000462172.1:n.*159C>T
ENST00000444639.5:c.*159C>T	ENSP00000463734.1:n.*159C>T
ENST00000545251.6:c.*159C>T	ENSP00000464040.1:n.*159C>T
ENST00000619513.1:c.76C>T	ENSP00000478803.1:p.Gln26Ter
NM_001162893.1:c.*159C>T	NP_001156365.1:n.*159C>T
NM_001162894.1:c.*159C>T	NP_001156366.1:n.*159C>T
NM_001162895.1:c.*159C>T	NP_001156367.1:n.*159C>T
NM_014656.2:c.*159C>T	NP_055471.2:n.*159C>T
XM_005245628.3:c.*159C>T	XP_005245685.1:n.*159C>T
XM_011510182.1:c.76C>T	XP_011508484.1:p.Gln26Ter
XM_011510183.1:c.76C>T	XP_011508485.1:p.Gln26Ter
XM_011510184.1:c.*159C>T	XP_011508486.1:n.*159C>T
NM_001319230.1:c.*159C>T	NP_001306159.1:n.*159C>T
NM_001319231.1:c.*159C>T	NP_001306160.1:n.*159C>T
XM_017002911.2:c.*159C>T	XP_016858400.1:n.*159C>T
NM_014656.3:c.*159C>T MANE Select	NP_055471.2:n.*159C>T
NM_001162893.2:c.*159C>T	NP_001156365.1:n.*159C>T
NM_001162894.2:c.*159C>T	NP_001156366.1:n.*159C>T
NM_001162895.2:c.*159C>T	NP_001156367.1:n.*159C>T
NM_001319230.2:c.*159C>T	NP_001306159.1:n.*159C>T
NM_001319231.2:c.*159C>T	NP_001306160.1:n.*159C>T