Canonical Allele Identifier: CA364218559

Gene: CUL7 KLC4

Linked Data

• MyVariant Identifiers: chr6:g.43015966G>T (hg19) ; chr6:g.43048228G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43048228G>T , CM000668.2:g.43048228G>T	GRCh38
NC_000006.11:g.43015966G>T , CM000668.1:g.43015966G>T	GRCh37
NC_000006.10:g.43123944G>T	NCBI36
NG_016205.1:g.10718C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674112.2:c.2089C>A (CUL7)	ENSP00000501166.2:p.Pro697Thr
ENST00000685042.1:c.2089C>A (CUL7)	ENSP00000509871.1:p.Pro697Thr
ENST00000686442.1:n.2372C>A (CUL7)
ENST00000687225.1:c.2185C>A (CUL7)	ENSP00000509364.1:p.Pro729Thr
ENST00000688302.1:n.2372C>A (CUL7)
ENST00000689256.1:n.2388C>A (CUL7)
ENST00000690231.1:c.2089C>A (CUL7)	ENSP00000508461.1:p.Pro697Thr
ENST00000265348.9:c.2089C>A (CUL7) MANE Select	ENSP00000265348.4:p.Pro697Thr
ENST00000673725.1:c.38C>A (CUL7)
ENST00000673753.1:n.2423C>A (CUL7)
ENST00000674100.1:c.2185C>A (CUL7)	ENSP00000501292.1:p.Pro729Thr
ENST00000674112.1:c.581C>A (CUL7)
ENST00000674134.1:c.2185C>A (CUL7)	ENSP00000501068.1:p.Pro729Thr
ENST00000265348.7:c.2089C>A (CUL7)	ENSP00000265348.3:p.Pro697Thr
ENST00000467906.5:c.-553+4720G>T (KLC4)	ENSP00000418759.1:n.-553+4720G>T
ENST00000535468.1:c.2341C>A (CUL7)	ENSP00000438788.1:p.Pro781Thr
NM_001168370.1:c.2341C>A (CUL7)	NP_001161842.1:p.Pro781Thr
NM_014780.4:c.2089C>A (CUL7)	NP_055595.2:p.Pro697Thr
XM_005249503.1:c.2245C>A (CUL7)	XP_005249560.1:p.Pro749Thr
XM_006715285.1:c.2185C>A (CUL7)	XP_006715348.1:p.Pro729Thr
XM_011515019.1:c.2341C>A (CUL7)	XP_011513321.1:p.Pro781Thr
XM_011515020.1:c.2245C>A (CUL7)	XP_011513322.1:p.Pro749Thr
XM_011515021.1:c.-94C>A (CUL7)	XP_011513323.1:n.-94C>A
XM_005249503.3:c.2245C>A (CUL7)	XP_005249560.1:p.Pro749Thr
XM_006715285.2:c.2185C>A (CUL7)	XP_006715348.1:p.Pro729Thr
XM_011515019.2:c.2341C>A (CUL7)	XP_011513321.1:p.Pro781Thr
XM_011515020.2:c.2245C>A (CUL7)	XP_011513322.1:p.Pro749Thr
XM_017011533.1:c.2368C>A (CUL7)	XP_016867022.1:p.Pro790Thr
XM_017011534.1:c.2368C>A (CUL7)	XP_016867023.1:p.Pro790Thr
XM_017011535.1:c.2272C>A (CUL7)	XP_016867024.1:p.Pro758Thr
XM_017011536.2:c.2212C>A (CUL7)	XP_016867025.1:p.Pro738Thr
XM_017011537.2:c.2185C>A (CUL7)	XP_016867026.1:p.Pro729Thr
XM_017011538.2:c.2116C>A (CUL7)	XP_016867027.1:p.Pro706Thr
XM_017011539.2:c.2089C>A (CUL7)	XP_016867028.1:p.Pro697Thr
XM_017011540.1:c.2368C>A (CUL7)	XP_016867029.1:p.Pro790Thr
NM_001168370.2:c.2185C>A (CUL7)	NP_001161842.2:p.Pro729Thr
NM_001374872.1:c.2185C>A (CUL7)	NP_001361801.1:p.Pro729Thr
NM_001374873.1:c.2089C>A (CUL7)	NP_001361802.1:p.Pro697Thr
NM_001374874.1:c.2089C>A (CUL7)	NP_001361803.1:p.Pro697Thr
NM_014780.5:c.2089C>A (CUL7) MANE Select	NP_055595.2:p.Pro697Thr