Canonical Allele Identifier: CA454141437
Gene: KLHL7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.23205550A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165931A>T , CM000669.2:g.23165931A>T GRCh38
NC_000007.13:g.23205550A>T , CM000669.1:g.23205550A>T GRCh37
NC_000007.12:g.23172075A>T NCBI36
NG_016983.1:g.65198A>T
NG_016983.2:g.65198A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1170A>T MANE Select ENSP00000343273.4:p.Ser390=
ENST00000339077.9:c.1170A>T ENSP00000343273.4:p.Ser390=
ENST00000409689.5:c.1026A>T ENSP00000386263.1:p.Ser342=
ENST00000469576.1:n.57A>T
ENST00000521082.5:c.*1178A>T ENSP00000430351.1:n.*1178A>T
NM_001031710.2:c.1170A>T NP_001026880.2:p.Ser390=
NM_018846.4:c.1026A>T NP_061334.4:p.Ser342=
NR_033328.1:n.1594A>T
XM_006715753.1:c.1209A>T XP_006715816.1:p.Ser403=
XM_006715754.1:c.1143A>T XP_006715817.1:p.Ser381=
XM_006715755.1:c.1143A>T XP_006715818.1:p.Ser381=
XM_006715756.1:c.1065A>T XP_006715819.1:p.Ser355=
XM_006715753.3:c.1209A>T XP_006715816.1:p.Ser403=
XM_006715754.3:c.1143A>T XP_006715817.1:p.Ser381=
XM_006715755.3:c.1143A>T XP_006715818.1:p.Ser381=
XM_006715756.3:c.1065A>T XP_006715819.1:p.Ser355=
XM_017012439.2:c.1104A>T XP_016867928.1:p.Ser368=
NM_001031710.3:c.1170A>T MANE Select NP_001026880.2:p.Ser390=
NM_018846.5:c.1026A>T NP_061334.4:p.Ser342=
NR_033328.2:n.1543A>T