Canonical Allele Identifier: CA2682028348
Gene: KLHL7 HGNC NCBI

Linked Data

gnomAD v4: 7-23165649-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165649A>G , CM000669.2:g.23165649A>G GRCh38
NC_000007.13:g.23205268A>G , CM000669.1:g.23205268A>G GRCh37
NC_000007.12:g.23171793A>G NCBI36
NG_016983.1:g.64916A>G
NG_016983.2:g.64916A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.937-49A>G MANE Select ENSP00000343273.4:n.937-49A>G
ENST00000339077.9:c.937-49A>G ENSP00000343273.4:n.937-49A>G
ENST00000409689.5:c.793-49A>G ENSP00000386263.1:n.793-49A>G
ENST00000521082.5:c.*945-49A>G ENSP00000430351.1:n.*945-49A>G
NM_001031710.2:c.937-49A>G NP_001026880.2:n.937-49A>G
NM_018846.4:c.793-49A>G NP_061334.4:n.793-49A>G
NR_033328.1:n.1361-49A>G
XM_006715753.1:c.976-49A>G XP_006715816.1:n.976-49A>G
XM_006715754.1:c.910-49A>G XP_006715817.1:n.910-49A>G
XM_006715755.1:c.910-49A>G XP_006715818.1:n.910-49A>G
XM_006715756.1:c.832-49A>G XP_006715819.1:n.832-49A>G
XM_006715753.3:c.976-49A>G XP_006715816.1:n.976-49A>G
XM_006715754.3:c.910-49A>G XP_006715817.1:n.910-49A>G
XM_006715755.3:c.910-49A>G XP_006715818.1:n.910-49A>G
XM_006715756.3:c.832-49A>G XP_006715819.1:n.832-49A>G
XM_017012439.2:c.871-49A>G XP_016867928.1:n.871-49A>G
NM_001031710.3:c.937-49A>G MANE Select NP_001026880.2:n.937-49A>G
NM_018846.5:c.793-49A>G NP_061334.4:n.793-49A>G
NR_033328.2:n.1310-49A>G