Canonical Allele Identifier: CA645548798
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165742_23165743insTTC , CM000669.2:g.23165742_23165743insTTC GRCh38
NC_000007.13:g.23205361_23205362insTTC , CM000669.1:g.23205361_23205362insTTC GRCh37
NC_000007.12:g.23171886_23171887insTTC NCBI36
NG_016983.1:g.65009_65010insTTC
NG_016983.2:g.65009_65010insTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.981_982insTTC MANE Select ENSP00000343273.4:p.Arg327_Asp328insPhe
ENST00000339077.9:c.981_982insTTC ENSP00000343273.4:p.Arg327_Asp328insPhe
ENST00000409689.5:c.837_838insTTC ENSP00000386263.1:p.Arg279_Asp280insPhe
ENST00000521082.5:c.*989_*990insTTC ENSP00000430351.1:n.*989_*990insTTC
NM_001031710.2:c.981_982insTTC NP_001026880.2:p.Arg327_Asp328insPhe
NM_018846.4:c.837_838insTTC NP_061334.4:p.Arg279_Asp280insPhe
NR_033328.1:n.1405_1406insTTC
XM_006715753.1:c.1020_1021insTTC XP_006715816.1:p.Arg340_Asp341insPhe
XM_006715754.1:c.954_955insTTC XP_006715817.1:p.Arg318_Asp319insPhe
XM_006715755.1:c.954_955insTTC XP_006715818.1:p.Arg318_Asp319insPhe
XM_006715756.1:c.876_877insTTC XP_006715819.1:p.Arg292_Asp293insPhe
XM_006715753.3:c.1020_1021insTTC XP_006715816.1:p.Arg340_Asp341insPhe
XM_006715754.3:c.954_955insTTC XP_006715817.1:p.Arg318_Asp319insPhe
XM_006715755.3:c.954_955insTTC XP_006715818.1:p.Arg318_Asp319insPhe
XM_006715756.3:c.876_877insTTC XP_006715819.1:p.Arg292_Asp293insPhe
XM_017012439.2:c.915_916insTTC XP_016867928.1:p.Arg305_Asp306insPhe
NM_001031710.3:c.981_982insTTC MANE Select NP_001026880.2:p.Arg327_Asp328insPhe
NM_018846.5:c.837_838insTTC NP_061334.4:p.Arg279_Asp280insPhe
NR_033328.2:n.1354_1355insTTC