Canonical Allele Identifier: CA16040629
Gene: KLHL24 HGNC NCBI

Linked Data

ClinVar Variation Id: 370042
dbSNP Id: rs1057515580

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183650358T>C , CM000665.2:g.183650358T>C GRCh38
NC_000003.11:g.183368146T>C , CM000665.1:g.183368146T>C GRCh37
NC_000003.10:g.184850840T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000242810.11:c.2T>C MANE Select ENSP00000242810.6:p.Met1Thr
ENST00000242810.10:c.2T>C ENSP00000242810.6:p.Met1Thr
ENST00000427201.2:c.2T>C ENSP00000408567.2:p.Met1Thr
ENST00000437402.5:c.2T>C ENSP00000408516.1:p.Met1Thr
ENST00000454495.6:c.2T>C ENSP00000416836.2:p.Met1Thr
ENST00000454652.6:c.2T>C ENSP00000395012.1:p.Met1Thr
ENST00000468001.1:c.2T>C ENSP00000418922.1:p.Met1Thr
ENST00000468101.5:c.2T>C ENSP00000420207.1:p.Met1Thr
ENST00000473045.5:c.2T>C ENSP00000419120.1:p.Met1Thr
ENST00000475827.5:n.152-13100T>C
ENST00000476808.1:c.2T>C ENSP00000419010.1:p.Met1Thr
ENST00000482138.1:c.2T>C ENSP00000417275.1:p.Met1Thr
ENST00000493074.1:c.2T>C ENSP00000417347.1:p.Met1Thr
NM_017644.3:c.2T>C MANE Select NP_060114.2:p.Met1Thr
XM_005247552.1:c.2T>C XP_005247609.1:p.Met1Thr
XM_005247553.1:c.2T>C XP_005247610.1:p.Met1Thr
XM_005247554.1:c.2T>C XP_005247611.1:p.Met1Thr
XM_005247555.1:c.2T>C XP_005247612.1:p.Met1Thr
XM_005247556.1:c.2T>C XP_005247613.1:p.Met1Thr
XM_006713674.1:c.2T>C XP_006713737.1:p.Met1Thr
XM_011512937.1:c.2T>C XP_011511239.1:p.Met1Thr
XM_011512938.1:c.2T>C XP_011511240.1:p.Met1Thr
XR_241499.2:n.282T>C
NM_001349413.1:c.2T>C NP_001336342.1:p.Met1Thr
NM_001349414.1:c.2T>C NP_001336343.1:p.Met1Thr
NM_001349415.1:c.2T>C NP_001336344.1:p.Met1Thr
NM_001349416.1:c.2T>C NP_001336345.1:p.Met1Thr
NM_001349417.1:c.2T>C NP_001336346.1:p.Met1Thr
NM_001349418.1:c.2T>C NP_001336347.1:p.Met1Thr
NM_001349419.1:c.2T>C NP_001336348.1:p.Met1Thr
NM_001349420.1:c.2T>C NP_001336349.1:p.Met1Thr
NM_001349421.1:c.2T>C NP_001336350.1:p.Met1Thr
NM_001349422.1:c.2T>C NP_001336351.1:p.Met1Thr
NM_001349423.1:c.2T>C NP_001336352.1:p.Met1Thr
NM_001349424.1:c.2T>C NP_001336353.1:p.Met1Thr
NM_001349425.1:c.2T>C NP_001336354.1:p.Met1Thr
NM_001349426.1:c.2T>C NP_001336355.1:p.Met1Thr
NM_001349428.1:c.-965T>C NP_001336357.1:n.-965T>C
NM_001349429.1:c.-965T>C NP_001336358.1:n.-965T>C
NR_146169.1:n.234T>C
NR_146170.1:n.297T>C
XM_005247552.2:c.2T>C XP_005247609.1:p.Met1Thr
XM_017006653.1:c.2T>C XP_016862142.1:p.Met1Thr
XM_017006655.1:c.2T>C XP_016862144.1:p.Met1Thr
XM_017006658.1:c.2T>C XP_016862147.1:p.Met1Thr
XM_017006661.1:c.-965T>C XP_016862150.1:n.-965T>C
XM_024453607.1:c.2T>C XP_024309375.1:p.Met1Thr