Canonical Allele Identifier: CA364228112

Gene: CUL7 KLC4

Linked Data

• MyVariant Identifiers: chr6:g.43019112G>A (hg19) ; chr6:g.43051374G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43051374G>A , CM000668.2:g.43051374G>A	GRCh38
NC_000006.11:g.43019112G>A , CM000668.1:g.43019112G>A	GRCh37
NC_000006.10:g.43127090G>A	NCBI36
NG_016205.1:g.7572C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674112.2:c.827C>T (CUL7)	ENSP00000501166.2:p.Ala276Val
ENST00000683160.1:n.1209C>T (CUL7)
ENST00000683493.1:n.868C>T (CUL7)
ENST00000685042.1:c.827C>T (CUL7)	ENSP00000509871.1:p.Ala276Val
ENST00000686442.1:n.1110C>T (CUL7)
ENST00000687225.1:c.923C>T (CUL7)	ENSP00000509364.1:p.Ala308Val
ENST00000688302.1:n.1110C>T (CUL7)
ENST00000688707.1:c.923C>T (CUL7)	ENSP00000510608.1:p.Ala308Val
ENST00000689256.1:n.1126C>T (CUL7)
ENST00000690231.1:c.827C>T (CUL7)	ENSP00000508461.1:p.Ala276Val
ENST00000265348.9:c.827C>T (CUL7) MANE Select	ENSP00000265348.4:p.Ala276Val
ENST00000673753.1:n.1161C>T (CUL7)
ENST00000673761.1:c.1578C>T	ENSP00000501018.1:n.1578C>T
ENST00000674100.1:c.923C>T (CUL7)	ENSP00000501292.1:p.Ala308Val
ENST00000674134.1:c.923C>T (CUL7)	ENSP00000501068.1:p.Ala308Val
ENST00000265348.7:c.827C>T (CUL7)	ENSP00000265348.3:p.Ala276Val
ENST00000467906.5:c.-552-7652G>A (KLC4)	ENSP00000418759.1:n.-552-7652G>A
ENST00000535468.1:c.1079C>T (CUL7)	ENSP00000438788.1:p.Ala360Val
NM_001168370.1:c.1079C>T (CUL7)	NP_001161842.1:p.Ala360Val
NM_014780.4:c.827C>T (CUL7)	NP_055595.2:p.Ala276Val
XM_005249503.1:c.983C>T (CUL7)	XP_005249560.1:p.Ala328Val
XM_006715285.1:c.923C>T (CUL7)	XP_006715348.1:p.Ala308Val
XM_011515019.1:c.1079C>T (CUL7)	XP_011513321.1:p.Ala360Val
XM_011515020.1:c.983C>T (CUL7)	XP_011513322.1:p.Ala328Val
XM_005249503.3:c.983C>T (CUL7)	XP_005249560.1:p.Ala328Val
XM_006715285.2:c.923C>T (CUL7)	XP_006715348.1:p.Ala308Val
XM_011515019.2:c.1079C>T (CUL7)	XP_011513321.1:p.Ala360Val
XM_011515020.2:c.983C>T (CUL7)	XP_011513322.1:p.Ala328Val
XM_017011533.1:c.1079C>T (CUL7)	XP_016867022.1:p.Ala360Val
XM_017011534.1:c.1079C>T (CUL7)	XP_016867023.1:p.Ala360Val
XM_017011535.1:c.983C>T (CUL7)	XP_016867024.1:p.Ala328Val
XM_017011536.2:c.923C>T (CUL7)	XP_016867025.1:p.Ala308Val
XM_017011537.2:c.923C>T (CUL7)	XP_016867026.1:p.Ala308Val
XM_017011538.2:c.827C>T (CUL7)	XP_016867027.1:p.Ala276Val
XM_017011539.2:c.827C>T (CUL7)	XP_016867028.1:p.Ala276Val
XM_017011540.1:c.1079C>T (CUL7)	XP_016867029.1:p.Ala360Val
NM_001168370.2:c.923C>T (CUL7)	NP_001161842.2:p.Ala308Val
NM_001374872.1:c.923C>T (CUL7)	NP_001361801.1:p.Ala308Val
NM_001374873.1:c.827C>T (CUL7)	NP_001361802.1:p.Ala276Val
NM_001374874.1:c.827C>T (CUL7)	NP_001361803.1:p.Ala276Val
NM_014780.5:c.827C>T (CUL7) MANE Select	NP_055595.2:p.Ala276Val