Canonical Allele Identifier: CA366981855

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23207544C>G (hg19) ; chr7:g.23167925C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23167925C>G , CM000669.2:g.23167925C>G	GRCh38
NC_000007.13:g.23207544C>G , CM000669.1:g.23207544C>G	GRCh37
NC_000007.12:g.23174069C>G	NCBI36
NG_016983.1:g.67192C>G
NG_016983.2:g.67192C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1267C>G MANE Select	ENSP00000343273.4:p.His423Asp
ENST00000339077.9:c.1267C>G	ENSP00000343273.4:p.His423Asp
ENST00000409689.5:c.1123C>G	ENSP00000386263.1:p.His375Asp
ENST00000469576.1:n.154C>G
ENST00000521082.5:c.*1275C>G	ENSP00000430351.1:n.*1275C>G
NM_001031710.2:c.1267C>G	NP_001026880.2:p.His423Asp
NM_018846.4:c.1123C>G	NP_061334.4:p.His375Asp
NR_033328.1:n.1691C>G
XM_006715753.1:c.1306C>G	XP_006715816.1:p.His436Asp
XM_006715754.1:c.1240C>G	XP_006715817.1:p.His414Asp
XM_006715755.1:c.1240C>G	XP_006715818.1:p.His414Asp
XM_006715756.1:c.1162C>G	XP_006715819.1:p.His388Asp
XM_006715753.3:c.1306C>G	XP_006715816.1:p.His436Asp
XM_006715754.3:c.1240C>G	XP_006715817.1:p.His414Asp
XM_006715755.3:c.1240C>G	XP_006715818.1:p.His414Asp
XM_006715756.3:c.1162C>G	XP_006715819.1:p.His388Asp
XM_017012439.2:c.1201C>G	XP_016867928.1:p.His401Asp
NM_001031710.3:c.1267C>G MANE Select	NP_001026880.2:p.His423Asp
NM_018846.5:c.1123C>G	NP_061334.4:p.His375Asp
NR_033328.2:n.1640C>G