Canonical Allele Identifier: CA2647139001
Gene: KCND3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111787166_111787167insGAAGC , CM000663.2:g.111787166_111787167insGAAGC GRCh38
NC_000001.10:g.112329788_112329789insGAAGC , CM000663.1:g.112329788_112329789insGAAGC GRCh37
NC_000001.9:g.112131311_112131312insGAAGC NCBI36
NG_032011.2:g.206989_206990insGCTTC , LRG_445:g.206989_206990insGCTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000302127.5:c.1107-61_1107-60insGCTTC MANE Select ENSP00000306923.4:n.1107-61_1107-60insGCTTC
ENST00000302127.4:c.1107-61_1107-60insGCTTC ENSP00000306923.3:n.1107-61_1107-60insGCTTC
ENST00000315987.6:c.1107-61_1107-60insGCTTC ENSP00000319591.2:n.1107-61_1107-60insGCTTC
ENST00000369697.5:c.1107-61_1107-60insGCTTC ENSP00000358711.1:n.1107-61_1107-60insGCTTC
NM_004980.4:c.1107-61_1107-60insGCTTC , LRG_445t1:c.1107-61_1107-60insGCTTC NP_004971.2:n.1107-61_1107-60insGCTTC
NM_172198.2:c.1107-61_1107-60insGCTTC NP_751948.1:n.1107-61_1107-60insGCTTC
XM_005270851.3:c.1107-61_1107-60insGCTTC XP_005270908.1:n.1107-61_1107-60insGCTTC
XM_006710629.2:c.1107-61_1107-60insGCTTC XP_006710692.1:n.1107-61_1107-60insGCTTC
XM_006710630.2:c.1107-61_1107-60insGCTTC XP_006710693.1:n.1107-61_1107-60insGCTTC
XM_006710631.2:c.1107-61_1107-60insGCTTC XP_006710694.1:n.1107-61_1107-60insGCTTC
XM_005270851.4:c.1107-61_1107-60insGCTTC XP_005270908.1:n.1107-61_1107-60insGCTTC
XM_006710629.4:c.1107-61_1107-60insGCTTC XP_006710692.1:n.1107-61_1107-60insGCTTC
XM_006710630.3:c.1107-61_1107-60insGCTTC XP_006710693.1:n.1107-61_1107-60insGCTTC
XM_006710631.3:c.1107-61_1107-60insGCTTC XP_006710694.1:n.1107-61_1107-60insGCTTC
XM_017001244.2:c.1107-61_1107-60insGCTTC XP_016856733.1:n.1107-61_1107-60insGCTTC
NM_001378969.1:c.1107-61_1107-60insGCTTC MANE Select NP_001365898.1:n.1107-61_1107-60insGCTTC
NM_001378970.1:c.1107-61_1107-60insGCTTC NP_001365899.1:n.1107-61_1107-60insGCTTC
NM_004980.5:c.1107-61_1107-60insGCTTC NP_004971.2:n.1107-61_1107-60insGCTTC
NM_172198.3:c.1107-61_1107-60insGCTTC NP_751948.1:n.1107-61_1107-60insGCTTC