Canonical Allele Identifier: CA389558062

Gene: KLHL28

Linked Data

• MyVariant Identifiers: chr14:g.45403709T>G (hg19) ; chr14:g.44934506T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44934506T>G , CM000676.2:g.44934506T>G	GRCh38
NC_000014.8:g.45403709T>G , CM000676.1:g.45403709T>G	GRCh37
NC_000014.7:g.44473459T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000396128.9:c.952A>C MANE Select	ENSP00000379434.4:p.Asn318His
ENST00000355081.3:c.994A>C	ENSP00000347193.2:p.Asn332His
ENST00000396128.8:c.952A>C	ENSP00000379434.3:p.Asn318His
NM_001308112.1:c.994A>C	NP_001295041.1:p.Asn332His
NM_017658.3:c.952A>C	NP_060128.2:p.Asn318His
NM_017658.4:c.952A>C	NP_060128.2:p.Asn318His
XM_005267770.2:c.952A>C	XP_005267827.1:p.Asn318His
XM_011536847.1:c.952A>C	XP_011535149.1:p.Asn318His
XM_011536848.1:c.952A>C	XP_011535150.1:p.Asn318His
XM_011536849.1:c.994A>C	XP_011535151.1:p.Asn332His
XM_005267770.4:c.952A>C	XP_005267827.1:p.Asn318His
XM_011536847.3:c.952A>C	XP_011535149.1:p.Asn318His
XM_011536849.2:c.994A>C	XP_011535151.1:p.Asn332His
XM_024449635.1:c.952A>C	XP_024305403.1:p.Asn318His
NM_001308112.2:c.994A>C	NP_001295041.1:p.Asn332His
NM_017658.5:c.952A>C MANE Select	NP_060128.2:p.Asn318His