Canonical Allele Identifier: CA1694330844
Gene: KLHL7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23166021G= , CM000669.2:g.23166021G= GRCh38
NC_000007.13:g.23205640G= , CM000669.1:g.23205640G= GRCh37
NC_000007.12:g.23172165G= NCBI36
NG_016983.1:g.65288G=
NG_016983.2:g.65288G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1177+83G= MANE Select ENSP00000343273.4:n.1177+83G=
ENST00000339077.9:c.1177+83G= ENSP00000343273.4:n.1177+83G=
ENST00000409689.5:c.1033+83G= ENSP00000386263.1:n.1033+83G=
ENST00000469576.1:n.64+83G=
ENST00000521082.5:c.*1185+83G= ENSP00000430351.1:n.*1185+83G=
NM_001031710.2:c.1177+83G= NP_001026880.2:n.1177+83G=
NM_018846.4:c.1033+83G= NP_061334.4:n.1033+83G=
NR_033328.1:n.1601+83G=
XM_006715753.1:c.1216+83G= XP_006715816.1:n.1216+83G=
XM_006715754.1:c.1150+83G= XP_006715817.1:n.1150+83G=
XM_006715755.1:c.1150+83G= XP_006715818.1:n.1150+83G=
XM_006715756.1:c.1072+83G= XP_006715819.1:n.1072+83G=
XM_006715753.3:c.1216+83G= XP_006715816.1:n.1216+83G=
XM_006715754.3:c.1150+83G= XP_006715817.1:n.1150+83G=
XM_006715755.3:c.1150+83G= XP_006715818.1:n.1150+83G=
XM_006715756.3:c.1072+83G= XP_006715819.1:n.1072+83G=
XM_017012439.2:c.1111+83G= XP_016867928.1:n.1111+83G=
NM_001031710.3:c.1177+83G= MANE Select NP_001026880.2:n.1177+83G=
NM_018846.5:c.1033+83G= NP_061334.4:n.1033+83G=
NR_033328.2:n.1550+83G=