Canonical Allele Identifier: CA1585511385
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137628244A= , CM000667.2:g.137628244A= GRCh38
NC_000005.9:g.136963933A= , CM000667.1:g.136963933A= GRCh37
NC_000005.8:g.136991832A= NCBI36
NG_032569.1:g.112847T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1591+53T= MANE Select ENSP00000312397.4:n.1591+53T=
ENST00000309755.8:c.1591+53T= ENSP00000312397.4:n.1591+53T=
ENST00000447439.6:n.1647+53T=
ENST00000504208.5:c.*475+53T= ENSP00000423585.1:n.*475+53T=
ENST00000506491.5:c.1345+53T= ENSP00000424828.1:n.1345+53T=
ENST00000506873.5:n.1114+53T=
ENST00000508657.5:c.1495+53T= ENSP00000422099.1:n.1495+53T=
ENST00000509694.1:n.437T=
NM_001257194.1:c.1495+53T= NP_001244123.1:n.1495+53T=
NM_001257195.1:c.1345+53T= NP_001244124.1:n.1345+53T=
NM_017415.2:c.1591+53T= NP_059111.2:n.1591+53T=
NM_017415.3:c.1591+53T= MANE Select NP_059111.2:n.1591+53T=
NM_001257195.2:c.1345+53T= NP_001244124.1:n.1345+53T=