Canonical Allele Identifier: CA364227641

Gene: CUL7 KLC4

Linked Data

• MyVariant Identifiers: chr6:g.43018949G>C (hg19) ; chr6:g.43051211G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43051211G>C , CM000668.2:g.43051211G>C	GRCh38
NC_000006.11:g.43018949G>C , CM000668.1:g.43018949G>C	GRCh37
NC_000006.10:g.43126927G>C	NCBI36
NG_016205.1:g.7735C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674112.2:c.990C>G (CUL7)	ENSP00000501166.2:p.Ile330Met
ENST00000683160.1:n.1372C>G (CUL7)
ENST00000683493.1:n.1031C>G (CUL7)
ENST00000685042.1:c.990C>G (CUL7)	ENSP00000509871.1:p.Ile330Met
ENST00000686442.1:n.1273C>G (CUL7)
ENST00000687225.1:c.1086C>G (CUL7)	ENSP00000509364.1:p.Ile362Met
ENST00000688302.1:n.1273C>G (CUL7)
ENST00000688707.1:c.1086C>G (CUL7)	ENSP00000510608.1:p.Ile362Met
ENST00000689256.1:n.1289C>G (CUL7)
ENST00000690231.1:c.990C>G (CUL7)	ENSP00000508461.1:p.Ile330Met
ENST00000265348.9:c.990C>G (CUL7) MANE Select	ENSP00000265348.4:p.Ile330Met
ENST00000673753.1:n.1324C>G (CUL7)
ENST00000673761.1:c.1741C>G	ENSP00000501018.1:n.1741C>G
ENST00000674100.1:c.1086C>G (CUL7)	ENSP00000501292.1:p.Ile362Met
ENST00000674134.1:c.1086C>G (CUL7)	ENSP00000501068.1:p.Ile362Met
ENST00000265348.7:c.990C>G (CUL7)	ENSP00000265348.3:p.Ile330Met
ENST00000467906.5:c.-553+7703G>C (KLC4)	ENSP00000418759.1:n.-553+7703G>C
ENST00000535468.1:c.1242C>G (CUL7)	ENSP00000438788.1:p.Ile414Met
NM_001168370.1:c.1242C>G (CUL7)	NP_001161842.1:p.Ile414Met
NM_014780.4:c.990C>G (CUL7)	NP_055595.2:p.Ile330Met
XM_005249503.1:c.1146C>G (CUL7)	XP_005249560.1:p.Ile382Met
XM_006715285.1:c.1086C>G (CUL7)	XP_006715348.1:p.Ile362Met
XM_011515019.1:c.1242C>G (CUL7)	XP_011513321.1:p.Ile414Met
XM_011515020.1:c.1146C>G (CUL7)	XP_011513322.1:p.Ile382Met
XM_005249503.3:c.1146C>G (CUL7)	XP_005249560.1:p.Ile382Met
XM_006715285.2:c.1086C>G (CUL7)	XP_006715348.1:p.Ile362Met
XM_011515019.2:c.1242C>G (CUL7)	XP_011513321.1:p.Ile414Met
XM_011515020.2:c.1146C>G (CUL7)	XP_011513322.1:p.Ile382Met
XM_017011533.1:c.1242C>G (CUL7)	XP_016867022.1:p.Ile414Met
XM_017011534.1:c.1242C>G (CUL7)	XP_016867023.1:p.Ile414Met
XM_017011535.1:c.1146C>G (CUL7)	XP_016867024.1:p.Ile382Met
XM_017011536.2:c.1086C>G (CUL7)	XP_016867025.1:p.Ile362Met
XM_017011537.2:c.1086C>G (CUL7)	XP_016867026.1:p.Ile362Met
XM_017011538.2:c.990C>G (CUL7)	XP_016867027.1:p.Ile330Met
XM_017011539.2:c.990C>G (CUL7)	XP_016867028.1:p.Ile330Met
XM_017011540.1:c.1242C>G (CUL7)	XP_016867029.1:p.Ile414Met
NM_001168370.2:c.1086C>G (CUL7)	NP_001161842.2:p.Ile362Met
NM_001374872.1:c.1086C>G (CUL7)	NP_001361801.1:p.Ile362Met
NM_001374873.1:c.990C>G (CUL7)	NP_001361802.1:p.Ile330Met
NM_001374874.1:c.990C>G (CUL7)	NP_001361803.1:p.Ile330Met
NM_014780.5:c.990C>G (CUL7) MANE Select	NP_055595.2:p.Ile330Met