Canonical Allele Identifier: CA1189065671

Gene: KCND3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111786895_111786915delinsTCCCCCGCATCCTTTACACTG , CM000663.2:g.111786895_111786915delinsTCCCCCGCATCCTTTACACTG	GRCh38
NC_000001.10:g.112329517_112329537delinsTCCCCCGCATCCTTTACACTG , CM000663.1:g.112329517_112329537delinsTCCCCCGCATCCTTTACACTG	GRCh37
NC_000001.9:g.112131040_112131060delinsTCCCCCGCATCCTTTACACTG	NCBI36
NG_032011.2:g.207241_207261delinsCAGTGTAAAGGATGCGGGGGA , LRG_445:g.207241_207261delinsCAGTGTAAAGGATGCGGGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302127.5:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA MANE Select	ENSP00000306923.4:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGG...
ENST00000302127.4:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	ENSP00000306923.3:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGG...
ENST00000315987.6:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	ENSP00000319591.2:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGG...
ENST00000369697.5:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	ENSP00000358711.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGG...
NM_004980.4:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA , LRG_445t1:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	NP_004971.2:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
NM_172198.2:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	NP_751948.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
XM_005270851.3:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	XP_005270908.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
XM_006710629.2:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	XP_006710692.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
XM_006710630.2:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	XP_006710693.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
XM_006710631.2:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	XP_006710694.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
XM_005270851.4:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	XP_005270908.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
XM_006710629.4:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	XP_006710692.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
XM_006710630.3:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	XP_006710693.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
XM_006710631.3:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	XP_006710694.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
XM_017001244.2:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	XP_016856733.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
NM_001378969.1:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA MANE Select	NP_001365898.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
NM_001378970.1:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	NP_001365899.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
NM_004980.5:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	NP_004971.2:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA
NM_172198.3:c.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA	NP_751948.1:n.1269+29_1269+49delinsCAGTGTAAAGGATGCGGGGGA