Canonical Allele Identifier: CA1694335284
Gene: KLHL7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23167840C= , CM000669.2:g.23167840C= GRCh38
NC_000007.13:g.23207459C= , CM000669.1:g.23207459C= GRCh37
NC_000007.12:g.23173984C= NCBI36
NG_016983.1:g.67107C=
NG_016983.2:g.67107C=

Transcript Alleles

HGVS Amino-acid change
ENST00000339077.10:c.1182C= MANE Select ENSP00000343273.4:p.Asn394=
ENST00000339077.9:c.1182C= ENSP00000343273.4:p.Asn394=
ENST00000409689.5:c.1038C= ENSP00000386263.1:p.Asn346=
ENST00000469576.1:n.69C=
ENST00000521082.5:c.*1190C= ENSP00000430351.1:n.*1190C=
NM_001031710.2:c.1182C= NP_001026880.2:p.Asn394=
NM_018846.4:c.1038C= NP_061334.4:p.Asn346=
NR_033328.1:n.1606C=
XM_006715753.1:c.1221C= XP_006715816.1:p.Asn407=
XM_006715754.1:c.1155C= XP_006715817.1:p.Asn385=
XM_006715755.1:c.1155C= XP_006715818.1:p.Asn385=
XM_006715756.1:c.1077C= XP_006715819.1:p.Asn359=
XM_006715753.3:c.1221C= XP_006715816.1:p.Asn407=
XM_006715754.3:c.1155C= XP_006715817.1:p.Asn385=
XM_006715755.3:c.1155C= XP_006715818.1:p.Asn385=
XM_006715756.3:c.1077C= XP_006715819.1:p.Asn359=
XM_017012439.2:c.1116C= XP_016867928.1:p.Asn372=
NM_001031710.3:c.1182C= MANE Select NP_001026880.2:p.Asn394=
NM_018846.5:c.1038C= NP_061334.4:p.Asn346=
NR_033328.2:n.1555C=