Canonical Allele Identifier: CA1694330728
Gene: KLHL7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165625_23165627delinsCTG , CM000669.2:g.23165625_23165627delinsCTG GRCh38
NC_000007.13:g.23205244_23205246delinsCTG , CM000669.1:g.23205244_23205246delinsCTG GRCh37
NC_000007.12:g.23171769_23171771delinsCTG NCBI36
NG_016983.1:g.64892_64894delinsCTG
NG_016983.2:g.64892_64894delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.937-73_937-71delinsCTG MANE Select ENSP00000343273.4:n.937-73_937-71delinsCTG
ENST00000339077.9:c.937-73_937-71delinsCTG ENSP00000343273.4:n.937-73_937-71delinsCTG
ENST00000409689.5:c.793-73_793-71delinsCTG ENSP00000386263.1:n.793-73_793-71delinsCTG
ENST00000521082.5:c.*945-73_*945-71delinsCTG ENSP00000430351.1:n.*945-73_*945-71delinsCTG
NM_001031710.2:c.937-73_937-71delinsCTG NP_001026880.2:n.937-73_937-71delinsCTG
NM_018846.4:c.793-73_793-71delinsCTG NP_061334.4:n.793-73_793-71delinsCTG
NR_033328.1:n.1361-73_1361-71delinsCTG
XM_006715753.1:c.976-73_976-71delinsCTG XP_006715816.1:n.976-73_976-71delinsCTG
XM_006715754.1:c.910-73_910-71delinsCTG XP_006715817.1:n.910-73_910-71delinsCTG
XM_006715755.1:c.910-73_910-71delinsCTG XP_006715818.1:n.910-73_910-71delinsCTG
XM_006715756.1:c.832-73_832-71delinsCTG XP_006715819.1:n.832-73_832-71delinsCTG
XM_006715753.3:c.976-73_976-71delinsCTG XP_006715816.1:n.976-73_976-71delinsCTG
XM_006715754.3:c.910-73_910-71delinsCTG XP_006715817.1:n.910-73_910-71delinsCTG
XM_006715755.3:c.910-73_910-71delinsCTG XP_006715818.1:n.910-73_910-71delinsCTG
XM_006715756.3:c.832-73_832-71delinsCTG XP_006715819.1:n.832-73_832-71delinsCTG
XM_017012439.2:c.871-73_871-71delinsCTG XP_016867928.1:n.871-73_871-71delinsCTG
NM_001031710.3:c.937-73_937-71delinsCTG MANE Select NP_001026880.2:n.937-73_937-71delinsCTG
NM_018846.5:c.793-73_793-71delinsCTG NP_061334.4:n.793-73_793-71delinsCTG
NR_033328.2:n.1310-73_1310-71delinsCTG