Canonical Allele Identifier: CA403986462

Gene: KEAP1

Linked Data

• dbSNP Id: rs1599482321
• MyVariant Identifiers: chr19:g.10600455A>T (hg19) ; chr19:g.10489779A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10489779A>T , CM000681.2:g.10489779A>T	GRCh38
NC_000019.9:g.10600455A>T , CM000681.1:g.10600455A>T	GRCh37
NC_000019.8:g.10461455A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000171111.10:c.1400T>A MANE Select	ENSP00000171111.4:p.Val467Asp
ENST00000171111.9:c.1400T>A	ENSP00000171111.4:p.Val467Asp
ENST00000393623.6:c.1400T>A	ENSP00000377245.1:p.Val467Asp
ENST00000590593.1:c.305-411T>A
ENST00000592478.5:c.219T>A
NM_012289.3:c.1400T>A	NP_036421.2:p.Val467Asp
NM_203500.1:c.1400T>A	NP_987096.1:p.Val467Asp
XM_005260173.1:c.1400T>A	XP_005260230.1:p.Val467Asp
XM_005260174.1:c.1400T>A	XP_005260231.1:p.Val467Asp
XM_011528452.1:c.1400T>A	XP_011526754.1:p.Val467Asp
NM_203500.2:c.1400T>A MANE Select	NP_987096.1:p.Val467Asp
NM_012289.4:c.1400T>A	NP_036421.2:p.Val467Asp