Canonical Allele Identifier: CA66534320

Gene: CUL3

Linked Data

• dbSNP Id: rs34441694
• MyVariant Identifiers: chr2:g.225368366_225368367insG (hg19) ; chr2:g.224503649_224503650insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503649_224503650insG , CM000664.2:g.224503649_224503650insG	GRCh38
NC_000002.11:g.225368366_225368367insG , CM000664.1:g.225368366_225368367insG	GRCh37
NC_000002.10:g.225076610_225076611insG	NCBI36
NG_032169.1:g.86748_86749insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1377+2_1377+3insC MANE Select	ENSP00000264414.4:n.1377+2_1377+3insC
ENST00000264414.8:c.1377+2_1377+3insC	ENSP00000264414.4:n.1377+2_1377+3insC
ENST00000344951.8:c.1179+2_1179+3insC	ENSP00000343601.4:n.1179+2_1179+3insC
ENST00000409096.5:c.1305+2_1305+3insC	ENSP00000387200.1:n.1305+2_1305+3insC
ENST00000409777.5:c.1305+2_1305+3insC	ENSP00000386525.1:n.1305+2_1305+3insC
ENST00000481135.1:n.673+2_673+3insC
ENST00000617432.4:c.99+2_99+3insC	ENSP00000477851.1:n.99+2_99+3insC
NM_001257197.1:c.1179+2_1179+3insC	NP_001244126.1:n.1179+2_1179+3insC
NM_001257198.1:c.1395+2_1395+3insC	NP_001244127.1:n.1395+2_1395+3insC
NM_003590.4:c.1377+2_1377+3insC	NP_003581.1:n.1377+2_1377+3insC
XM_006712800.2:c.1344+2_1344+3insC	XP_006712863.2:n.1344+2_1344+3insC
XM_011511994.1:c.1230+2_1230+3insC	XP_011510296.1:n.1230+2_1230+3insC
XM_011511995.1:c.1335+2_1335+3insC	XP_011510297.1:n.1335+2_1335+3insC
XM_011511996.1:c.1185+2_1185+3insC	XP_011510298.1:n.1185+2_1185+3insC
XM_011511997.1:c.1077+2_1077+3insC	XP_011510299.1:n.1077+2_1077+3insC
XM_011511994.3:c.1230+2_1230+3insC	XP_011510296.1:n.1230+2_1230+3insC
XM_011511996.2:c.1185+2_1185+3insC	XP_011510298.1:n.1185+2_1185+3insC
NM_003590.5:c.1377+2_1377+3insC MANE Select	NP_003581.1:n.1377+2_1377+3insC
NM_001257198.2:c.1395+2_1395+3insC	NP_001244127.1:n.1395+2_1395+3insC
NM_001257197.2:c.1179+2_1179+3insC	NP_001244126.1:n.1179+2_1179+3insC