Canonical Allele Identifier: CA1624357089

Gene: CUL7 KLC4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43047890_43047891delinsGT , CM000668.2:g.43047890_43047891delinsGT	GRCh38
NC_000006.11:g.43015628_43015629delinsGT , CM000668.1:g.43015628_43015629delinsGT	GRCh37
NC_000006.10:g.43123606_43123607delinsGT	NCBI36
NG_016205.1:g.11055_11056delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478630.2:n.56+56_56+57delinsAC (CUL7)
ENST00000674112.2:c.2169+257_2169+258delinsAC (CUL7)	ENSP00000501166.2:n.2169+257_2169+258delinsAC
ENST00000685042.1:c.2169+257_2169+258delinsAC (CUL7)	ENSP00000509871.1:n.2169+257_2169+258delinsAC
ENST00000686442.1:n.2452+257_2452+258delinsAC (CUL7)
ENST00000687225.1:c.*4+56_*4+57delinsAC (CUL7)	ENSP00000509364.1:n.*4+56_*4+57delinsAC
ENST00000688302.1:n.2452+257_2452+258delinsAC (CUL7)
ENST00000689256.1:n.2468+257_2468+258delinsAC (CUL7)
ENST00000690231.1:c.2169+257_2169+258delinsAC (CUL7)	ENSP00000508461.1:n.2169+257_2169+258delinsAC
ENST00000265348.9:c.2169+257_2169+258delinsAC (CUL7) MANE Select	ENSP00000265348.4:n.2169+257_2169+258delinsAC
ENST00000673725.1:c.118+257_118+258delinsAC (CUL7)
ENST00000673753.1:n.2546+56_2546+57delinsAC (CUL7)
ENST00000674100.1:c.2265+257_2265+258delinsAC (CUL7)	ENSP00000501292.1:n.2265+257_2265+258delinsAC
ENST00000674112.1:c.661+257_661+258delinsAC (CUL7)
ENST00000674134.1:c.2265+257_2265+258delinsAC (CUL7)	ENSP00000501068.1:n.2265+257_2265+258delinsAC
ENST00000265348.7:c.2169+257_2169+258delinsAC (CUL7)	ENSP00000265348.3:n.2169+257_2169+258delinsAC
ENST00000467906.5:c.-553+4382_-553+4383delinsGT (KLC4)	ENSP00000418759.1:n.-553+4382_-553+4383delinsGT
ENST00000478630.1:n.56+56_56+57delinsAC (CUL7)
ENST00000535468.1:c.2421+257_2421+258delinsAC (CUL7)	ENSP00000438788.1:n.2421+257_2421+258delinsAC
NM_001168370.1:c.2421+257_2421+258delinsAC (CUL7)	NP_001161842.1:n.2421+257_2421+258delinsAC
NM_014780.4:c.2169+257_2169+258delinsAC (CUL7)	NP_055595.2:n.2169+257_2169+258delinsAC
XM_005249503.1:c.2325+257_2325+258delinsAC (CUL7)	XP_005249560.1:n.2325+257_2325+258delinsAC
XM_006715285.1:c.2265+257_2265+258delinsAC (CUL7)	XP_006715348.1:n.2265+257_2265+258delinsAC
XM_011515019.1:c.2421+257_2421+258delinsAC (CUL7)	XP_011513321.1:n.2421+257_2421+258delinsAC
XM_011515020.1:c.2325+257_2325+258delinsAC (CUL7)	XP_011513322.1:n.2325+257_2325+258delinsAC
XM_011515021.1:c.30+56_30+57delinsAC (CUL7)	XP_011513323.1:n.30+56_30+57delinsAC
XM_005249503.3:c.2325+257_2325+258delinsAC (CUL7)	XP_005249560.1:n.2325+257_2325+258delinsAC
XM_006715285.2:c.2265+257_2265+258delinsAC (CUL7)	XP_006715348.1:n.2265+257_2265+258delinsAC
XM_011515019.2:c.2421+257_2421+258delinsAC (CUL7)	XP_011513321.1:n.2421+257_2421+258delinsAC
XM_011515020.2:c.2325+257_2325+258delinsAC (CUL7)	XP_011513322.1:n.2325+257_2325+258delinsAC
XM_017011533.1:c.2448+257_2448+258delinsAC (CUL7)	XP_016867022.1:n.2448+257_2448+258delinsAC
XM_017011534.1:c.2448+257_2448+258delinsAC (CUL7)	XP_016867023.1:n.2448+257_2448+258delinsAC
XM_017011535.1:c.2352+257_2352+258delinsAC (CUL7)	XP_016867024.1:n.2352+257_2352+258delinsAC
XM_017011536.2:c.2292+257_2292+258delinsAC (CUL7)	XP_016867025.1:n.2292+257_2292+258delinsAC
XM_017011537.2:c.2265+257_2265+258delinsAC (CUL7)	XP_016867026.1:n.2265+257_2265+258delinsAC
XM_017011538.2:c.2196+257_2196+258delinsAC (CUL7)	XP_016867027.1:n.2196+257_2196+258delinsAC
XM_017011539.2:c.2169+257_2169+258delinsAC (CUL7)	XP_016867028.1:n.2169+257_2169+258delinsAC
XM_017011540.1:c.2448+257_2448+258delinsAC (CUL7)	XP_016867029.1:n.2448+257_2448+258delinsAC
NM_001168370.2:c.2265+257_2265+258delinsAC (CUL7)	NP_001161842.2:n.2265+257_2265+258delinsAC
NM_001374872.1:c.2265+257_2265+258delinsAC (CUL7)	NP_001361801.1:n.2265+257_2265+258delinsAC
NM_001374873.1:c.2169+257_2169+258delinsAC (CUL7)	NP_001361802.1:n.2169+257_2169+258delinsAC
NM_001374874.1:c.2169+257_2169+258delinsAC (CUL7)	NP_001361803.1:n.2169+257_2169+258delinsAC
NM_014780.5:c.2169+257_2169+258delinsAC (CUL7) MANE Select	NP_055595.2:n.2169+257_2169+258delinsAC