Canonical Allele Identifier: CA389557696

Gene: KLHL28

Linked Data

• MyVariant Identifiers: chr14:g.45403622C>A (hg19) ; chr14:g.44934419C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44934419C>A , CM000676.2:g.44934419C>A	GRCh38
NC_000014.8:g.45403622C>A , CM000676.1:g.45403622C>A	GRCh37
NC_000014.7:g.44473372C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396128.9:c.1039G>T MANE Select	ENSP00000379434.4:p.Val347Phe
ENST00000355081.3:c.1081G>T	ENSP00000347193.2:p.Val361Phe
ENST00000396128.8:c.1039G>T	ENSP00000379434.3:p.Val347Phe
NM_001308112.1:c.1081G>T	NP_001295041.1:p.Val361Phe
NM_017658.3:c.1039G>T	NP_060128.2:p.Val347Phe
NM_017658.4:c.1039G>T	NP_060128.2:p.Val347Phe
XM_005267770.2:c.1039G>T	XP_005267827.1:p.Val347Phe
XM_011536847.1:c.1039G>T	XP_011535149.1:p.Val347Phe
XM_011536848.1:c.1039G>T	XP_011535150.1:p.Val347Phe
XM_011536849.1:c.1081G>T	XP_011535151.1:p.Val361Phe
XM_005267770.4:c.1039G>T	XP_005267827.1:p.Val347Phe
XM_011536847.3:c.1039G>T	XP_011535149.1:p.Val347Phe
XM_011536849.2:c.1081G>T	XP_011535151.1:p.Val361Phe
XM_024449635.1:c.1039G>T	XP_024305403.1:p.Val347Phe
NM_001308112.2:c.1081G>T	NP_001295041.1:p.Val361Phe
NM_017658.5:c.1039G>T MANE Select	NP_060128.2:p.Val347Phe