Canonical Allele Identifier: CA389558037

Gene: KLHL28

Linked Data

• MyVariant Identifiers: chr14:g.45403704A>C (hg19) ; chr14:g.44934501A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44934501A>C , CM000676.2:g.44934501A>C	GRCh38
NC_000014.8:g.45403704A>C , CM000676.1:g.45403704A>C	GRCh37
NC_000014.7:g.44473454A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000396128.9:c.957T>G MANE Select	ENSP00000379434.4:p.Ile319Met
ENST00000355081.3:c.999T>G	ENSP00000347193.2:p.Ile333Met
ENST00000396128.8:c.957T>G	ENSP00000379434.3:p.Ile319Met
NM_001308112.1:c.999T>G	NP_001295041.1:p.Ile333Met
NM_017658.3:c.957T>G	NP_060128.2:p.Ile319Met
NM_017658.4:c.957T>G	NP_060128.2:p.Ile319Met
XM_005267770.2:c.957T>G	XP_005267827.1:p.Ile319Met
XM_011536847.1:c.957T>G	XP_011535149.1:p.Ile319Met
XM_011536848.1:c.957T>G	XP_011535150.1:p.Ile319Met
XM_011536849.1:c.999T>G	XP_011535151.1:p.Ile333Met
XM_005267770.4:c.957T>G	XP_005267827.1:p.Ile319Met
XM_011536847.3:c.957T>G	XP_011535149.1:p.Ile319Met
XM_011536849.2:c.999T>G	XP_011535151.1:p.Ile333Met
XM_024449635.1:c.957T>G	XP_024305403.1:p.Ile319Met
NM_001308112.2:c.999T>G	NP_001295041.1:p.Ile333Met
NM_017658.5:c.957T>G MANE Select	NP_060128.2:p.Ile319Met