Canonical Allele Identifier: CA2682028375
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23166015dup , CM000669.2:g.23166015dup GRCh38
NC_000007.13:g.23205634dup , CM000669.1:g.23205634dup GRCh37
NC_000007.12:g.23172159dup NCBI36
NG_016983.1:g.65282dup
NG_016983.2:g.65282dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1177+77dup MANE Select ENSP00000343273.4:n.1177+77dup
ENST00000339077.9:c.1177+77dup ENSP00000343273.4:n.1177+77dup
ENST00000409689.5:c.1033+77dup ENSP00000386263.1:n.1033+77dup
ENST00000469576.1:n.64+77dup
ENST00000521082.5:c.*1185+77dup ENSP00000430351.1:n.*1185+77dup
NM_001031710.2:c.1177+77dup NP_001026880.2:n.1177+77dup
NM_018846.4:c.1033+77dup NP_061334.4:n.1033+77dup
NR_033328.1:n.1601+77dup
XM_006715753.1:c.1216+77dup XP_006715816.1:n.1216+77dup
XM_006715754.1:c.1150+77dup XP_006715817.1:n.1150+77dup
XM_006715755.1:c.1150+77dup XP_006715818.1:n.1150+77dup
XM_006715756.1:c.1072+77dup XP_006715819.1:n.1072+77dup
XM_006715753.3:c.1216+77dup XP_006715816.1:n.1216+77dup
XM_006715754.3:c.1150+77dup XP_006715817.1:n.1150+77dup
XM_006715755.3:c.1150+77dup XP_006715818.1:n.1150+77dup
XM_006715756.3:c.1072+77dup XP_006715819.1:n.1072+77dup
XM_017012439.2:c.1111+77dup XP_016867928.1:n.1111+77dup
NM_001031710.3:c.1177+77dup MANE Select NP_001026880.2:n.1177+77dup
NM_018846.5:c.1033+77dup NP_061334.4:n.1033+77dup
NR_033328.2:n.1550+77dup