Canonical Allele Identifier: CA366981256
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165769T>G , CM000669.2:g.23165769T>G GRCh38
NC_000007.13:g.23205388T>G , CM000669.1:g.23205388T>G GRCh37
NC_000007.12:g.23171913T>G NCBI36
NG_016983.1:g.65036T>G
NG_016983.2:g.65036T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1008T>G MANE Select ENSP00000343273.4:p.Asn336Lys
ENST00000339077.9:c.1008T>G ENSP00000343273.4:p.Asn336Lys
ENST00000409689.5:c.864T>G ENSP00000386263.1:p.Asn288Lys
ENST00000521082.5:c.*1016T>G ENSP00000430351.1:n.*1016T>G
NM_001031710.2:c.1008T>G NP_001026880.2:p.Asn336Lys
NM_018846.4:c.864T>G NP_061334.4:p.Asn288Lys
NR_033328.1:n.1432T>G
XM_006715753.1:c.1047T>G XP_006715816.1:p.Asn349Lys
XM_006715754.1:c.981T>G XP_006715817.1:p.Asn327Lys
XM_006715755.1:c.981T>G XP_006715818.1:p.Asn327Lys
XM_006715756.1:c.903T>G XP_006715819.1:p.Asn301Lys
XM_006715753.3:c.1047T>G XP_006715816.1:p.Asn349Lys
XM_006715754.3:c.981T>G XP_006715817.1:p.Asn327Lys
XM_006715755.3:c.981T>G XP_006715818.1:p.Asn327Lys
XM_006715756.3:c.903T>G XP_006715819.1:p.Asn301Lys
XM_017012439.2:c.942T>G XP_016867928.1:p.Asn314Lys
NM_001031710.3:c.1008T>G MANE Select NP_001026880.2:p.Asn336Lys
NM_018846.5:c.864T>G NP_061334.4:p.Asn288Lys
NR_033328.2:n.1381T>G