Canonical Allele Identifier: CA3422292

Gene: KLHL3

Linked Data

• dbSNP Id: rs373765961
• ExAC: 5:136974757 G / A
• gnomAD v2: 5-136974757-G-A
• gnomAD v3: 5-137639068-G-A
• gnomAD v4: 5-137639068-G-A
• COSMIC: COSM481966
• MyVariant Identifiers: chr5:g.136974757G>A (hg19) ; chr5:g.137639068G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639068G>A , CM000667.2:g.137639068G>A	GRCh38
NC_000005.9:g.136974757G>A , CM000667.1:g.136974757G>A	GRCh37
NC_000005.8:g.137002656G>A	NCBI36
NG_032569.1:g.102023C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1104C>T MANE Select	ENSP00000312397.4:p.Asp368=
ENST00000309755.8:c.1104C>T	ENSP00000312397.4:p.Asp368=
ENST00000502381.1:n.691C>T
ENST00000504208.5:c.*335-10631C>T	ENSP00000423585.1:n.*335-10631C>T
ENST00000505853.1:c.984C>T	ENSP00000426173.1:p.Asp328=
ENST00000506491.5:c.858C>T	ENSP00000424828.1:p.Asp286=
ENST00000506873.5:n.729C>T
ENST00000508657.5:c.1008C>T	ENSP00000422099.1:p.Asp336=
NM_001257194.1:c.1008C>T	NP_001244123.1:p.Asp336=
NM_001257195.1:c.858C>T	NP_001244124.1:p.Asp286=
NM_017415.2:c.1104C>T	NP_059111.2:p.Asp368=
NM_017415.3:c.1104C>T MANE Select	NP_059111.2:p.Asp368=
NM_001257195.2:c.858C>T	NP_001244124.1:p.Asp286=