Canonical Allele Identifier: CA389558129

Gene: KLHL28

Linked Data

• MyVariant Identifiers: chr14:g.45403727T>A (hg19) ; chr14:g.44934524T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44934524T>A , CM000676.2:g.44934524T>A	GRCh38
NC_000014.8:g.45403727T>A , CM000676.1:g.45403727T>A	GRCh37
NC_000014.7:g.44473477T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396128.9:c.934A>T MANE Select	ENSP00000379434.4:p.Ile312Phe
ENST00000355081.3:c.976A>T	ENSP00000347193.2:p.Ile326Phe
ENST00000396128.8:c.934A>T	ENSP00000379434.3:p.Ile312Phe
NM_001308112.1:c.976A>T	NP_001295041.1:p.Ile326Phe
NM_017658.3:c.934A>T	NP_060128.2:p.Ile312Phe
NM_017658.4:c.934A>T	NP_060128.2:p.Ile312Phe
XM_005267770.2:c.934A>T	XP_005267827.1:p.Ile312Phe
XM_011536847.1:c.934A>T	XP_011535149.1:p.Ile312Phe
XM_011536848.1:c.934A>T	XP_011535150.1:p.Ile312Phe
XM_011536849.1:c.976A>T	XP_011535151.1:p.Ile326Phe
XM_005267770.4:c.934A>T	XP_005267827.1:p.Ile312Phe
XM_011536847.3:c.934A>T	XP_011535149.1:p.Ile312Phe
XM_011536849.2:c.976A>T	XP_011535151.1:p.Ile326Phe
XM_024449635.1:c.934A>T	XP_024305403.1:p.Ile312Phe
NM_001308112.2:c.976A>T	NP_001295041.1:p.Ile326Phe
NM_017658.5:c.934A>T MANE Select	NP_060128.2:p.Ile312Phe