Canonical Allele Identifier: CA361045528

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136964036G>A (hg19) ; chr5:g.137628347G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137628347G>A , CM000667.2:g.137628347G>A	GRCh38
NC_000005.9:g.136964036G>A , CM000667.1:g.136964036G>A	GRCh37
NC_000005.8:g.136991935G>A	NCBI36
NG_032569.1:g.112744C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1541C>T MANE Select	ENSP00000312397.4:p.Thr514Ile
ENST00000309755.8:c.1541C>T	ENSP00000312397.4:p.Thr514Ile
ENST00000447439.6:n.1597C>T
ENST00000504208.5:c.*425C>T	ENSP00000423585.1:n.*425C>T
ENST00000506491.5:c.1295C>T	ENSP00000424828.1:p.Thr432Ile
ENST00000506873.5:n.1064C>T
ENST00000508657.5:c.1445C>T	ENSP00000422099.1:p.Thr482Ile
ENST00000509694.1:n.334C>T
NM_001257194.1:c.1445C>T	NP_001244123.1:p.Thr482Ile
NM_001257195.1:c.1295C>T	NP_001244124.1:p.Thr432Ile
NM_017415.2:c.1541C>T	NP_059111.2:p.Thr514Ile
NM_017415.3:c.1541C>T MANE Select	NP_059111.2:p.Thr514Ile
NM_001257195.2:c.1295C>T	NP_001244124.1:p.Thr432Ile