Canonical Allele Identifier: CA1585511233
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137627935T= , CM000667.2:g.137627935T= GRCh38
NC_000005.9:g.136963624T= , CM000667.1:g.136963624T= GRCh37
NC_000005.8:g.136991523T= NCBI36
NG_032569.1:g.113156A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1591+362A= MANE Select ENSP00000312397.4:n.1591+362A=
ENST00000309755.8:c.1591+362A= ENSP00000312397.4:n.1591+362A=
ENST00000447439.6:n.1647+362A=
ENST00000504208.5:c.*475+362A= ENSP00000423585.1:n.*475+362A=
ENST00000506491.5:c.1345+362A= ENSP00000424828.1:n.1345+362A=
ENST00000506873.5:n.1114+362A=
ENST00000508657.5:c.1495+362A= ENSP00000422099.1:n.1495+362A=
ENST00000509694.1:n.622+124A=
NM_001257194.1:c.1495+362A= NP_001244123.1:n.1495+362A=
NM_001257195.1:c.1345+362A= NP_001244124.1:n.1345+362A=
NM_017415.2:c.1591+362A= NP_059111.2:n.1591+362A=
NM_017415.3:c.1591+362A= MANE Select NP_059111.2:n.1591+362A=
NM_001257195.2:c.1345+362A= NP_001244124.1:n.1345+362A=