Canonical Allele Identifier: CA1694330813
Gene: KLHL7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165908A= , CM000669.2:g.23165908A= GRCh38
NC_000007.13:g.23205527A= , CM000669.1:g.23205527A= GRCh37
NC_000007.12:g.23172052A= NCBI36
NG_016983.1:g.65175A=
NG_016983.2:g.65175A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1147A= MANE Select ENSP00000343273.4:p.Lys383=
ENST00000339077.9:c.1147A= ENSP00000343273.4:p.Lys383=
ENST00000409689.5:c.1003A= ENSP00000386263.1:p.Lys335=
ENST00000469576.1:n.34A=
ENST00000521082.5:c.*1155A= ENSP00000430351.1:n.*1155A=
NM_001031710.2:c.1147A= NP_001026880.2:p.Lys383=
NM_018846.4:c.1003A= NP_061334.4:p.Lys335=
NR_033328.1:n.1571A=
XM_006715753.1:c.1186A= XP_006715816.1:p.Lys396=
XM_006715754.1:c.1120A= XP_006715817.1:p.Lys374=
XM_006715755.1:c.1120A= XP_006715818.1:p.Lys374=
XM_006715756.1:c.1042A= XP_006715819.1:p.Lys348=
XM_006715753.3:c.1186A= XP_006715816.1:p.Lys396=
XM_006715754.3:c.1120A= XP_006715817.1:p.Lys374=
XM_006715755.3:c.1120A= XP_006715818.1:p.Lys374=
XM_006715756.3:c.1042A= XP_006715819.1:p.Lys348=
XM_017012439.2:c.1081A= XP_016867928.1:p.Lys361=
NM_001031710.3:c.1147A= MANE Select NP_001026880.2:p.Lys383=
NM_018846.5:c.1003A= NP_061334.4:p.Lys335=
NR_033328.2:n.1520A=