Canonical Allele Identifier: CA364218522

Gene: CUL7 KLC4

Linked Data

• MyVariant Identifiers: chr6:g.43015960C>T (hg19) ; chr6:g.43048222C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43048222C>T , CM000668.2:g.43048222C>T	GRCh38
NC_000006.11:g.43015960C>T , CM000668.1:g.43015960C>T	GRCh37
NC_000006.10:g.43123938C>T	NCBI36
NG_016205.1:g.10724G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674112.2:c.2095G>A (CUL7)	ENSP00000501166.2:p.Ala699Thr
ENST00000685042.1:c.2095G>A (CUL7)	ENSP00000509871.1:p.Ala699Thr
ENST00000686442.1:n.2378G>A (CUL7)
ENST00000687225.1:c.2191G>A (CUL7)	ENSP00000509364.1:p.Ala731Thr
ENST00000688302.1:n.2378G>A (CUL7)
ENST00000689256.1:n.2394G>A (CUL7)
ENST00000690231.1:c.2095G>A (CUL7)	ENSP00000508461.1:p.Ala699Thr
ENST00000265348.9:c.2095G>A (CUL7) MANE Select	ENSP00000265348.4:p.Ala699Thr
ENST00000673725.1:c.44G>A (CUL7)
ENST00000673753.1:n.2429G>A (CUL7)
ENST00000674100.1:c.2191G>A (CUL7)	ENSP00000501292.1:p.Ala731Thr
ENST00000674112.1:c.587G>A (CUL7)
ENST00000674134.1:c.2191G>A (CUL7)	ENSP00000501068.1:p.Ala731Thr
ENST00000265348.7:c.2095G>A (CUL7)	ENSP00000265348.3:p.Ala699Thr
ENST00000467906.5:c.-553+4714C>T (KLC4)	ENSP00000418759.1:n.-553+4714C>T
ENST00000535468.1:c.2347G>A (CUL7)	ENSP00000438788.1:p.Ala783Thr
NM_001168370.1:c.2347G>A (CUL7)	NP_001161842.1:p.Ala783Thr
NM_014780.4:c.2095G>A (CUL7)	NP_055595.2:p.Ala699Thr
XM_005249503.1:c.2251G>A (CUL7)	XP_005249560.1:p.Ala751Thr
XM_006715285.1:c.2191G>A (CUL7)	XP_006715348.1:p.Ala731Thr
XM_011515019.1:c.2347G>A (CUL7)	XP_011513321.1:p.Ala783Thr
XM_011515020.1:c.2251G>A (CUL7)	XP_011513322.1:p.Ala751Thr
XM_011515021.1:c.-88G>A (CUL7)	XP_011513323.1:n.-88G>A
XM_005249503.3:c.2251G>A (CUL7)	XP_005249560.1:p.Ala751Thr
XM_006715285.2:c.2191G>A (CUL7)	XP_006715348.1:p.Ala731Thr
XM_011515019.2:c.2347G>A (CUL7)	XP_011513321.1:p.Ala783Thr
XM_011515020.2:c.2251G>A (CUL7)	XP_011513322.1:p.Ala751Thr
XM_017011533.1:c.2374G>A (CUL7)	XP_016867022.1:p.Ala792Thr
XM_017011534.1:c.2374G>A (CUL7)	XP_016867023.1:p.Ala792Thr
XM_017011535.1:c.2278G>A (CUL7)	XP_016867024.1:p.Ala760Thr
XM_017011536.2:c.2218G>A (CUL7)	XP_016867025.1:p.Ala740Thr
XM_017011537.2:c.2191G>A (CUL7)	XP_016867026.1:p.Ala731Thr
XM_017011538.2:c.2122G>A (CUL7)	XP_016867027.1:p.Ala708Thr
XM_017011539.2:c.2095G>A (CUL7)	XP_016867028.1:p.Ala699Thr
XM_017011540.1:c.2374G>A (CUL7)	XP_016867029.1:p.Ala792Thr
NM_001168370.2:c.2191G>A (CUL7)	NP_001161842.2:p.Ala731Thr
NM_001374872.1:c.2191G>A (CUL7)	NP_001361801.1:p.Ala731Thr
NM_001374873.1:c.2095G>A (CUL7)	NP_001361802.1:p.Ala699Thr
NM_001374874.1:c.2095G>A (CUL7)	NP_001361803.1:p.Ala699Thr
NM_014780.5:c.2095G>A (CUL7) MANE Select	NP_055595.2:p.Ala699Thr