Canonical Allele Identifier: CA2454909259

Gene: CUL4B

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120560228C= , CM000685.2:g.120560228C=	GRCh38
NC_000023.10:g.119694083C= , CM000685.1:g.119694083C=	GRCh37
NC_000023.9:g.119578111C=	NCBI36
NG_009388.1:g.20602G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336592.11:c.426G=	ENSP00000338919.6:p.Gln142=
ENST00000371322.11:c.411G= MANE Select	ENSP00000360373.5:p.Gln137=
ENST00000404115.8:c.411G=	ENSP00000384109.4:p.Gln137=
ENST00000467641.2:n.78G=
ENST00000673919.1:c.411G=	ENSP00000500994.1:p.Gln137=
ENST00000674137.11:c.411G=	ENSP00000501019.6:p.Gln137=
ENST00000679432.1:c.398G=
ENST00000679927.1:c.66G=	ENSP00000505603.1:p.Gln22=
ENST00000680165.1:n.737G=
ENST00000680324.1:n.325G=
ENST00000680577.1:n.572G=
ENST00000680673.1:c.465G=	ENSP00000505084.1:p.Gln155=
ENST00000681090.1:c.411G=	ENSP00000506288.1:p.Gln137=
ENST00000681206.1:c.426G=	ENSP00000505480.1:p.Gln142=
ENST00000681253.1:c.465G=	ENSP00000506259.1:p.Gln155=
ENST00000681333.1:c.411G=	ENSP00000505739.1:p.Gln137=
ENST00000681652.1:c.465G=	ENSP00000505176.1:p.Gln155=
ENST00000336592.10:c.426G=	ENSP00000338919.6:p.Gln142=
ENST00000371322.9:c.411G=	ENSP00000360373.5:p.Gln137=
ENST00000404115.7:c.465G=	ENSP00000384109.3:p.Gln155=
ENST00000467641.1:n.568G=
NM_001079872.1:c.411G=	NP_001073341.1:p.Gln137=
NM_003588.3:c.465G=	NP_003579.3:p.Gln155=
XM_005262481.1:c.465G=	XP_005262538.1:p.Gln155=
XM_006724784.1:c.426G=	XP_006724847.1:p.Gln142=
XM_006724785.1:c.426G=	XP_006724848.1:p.Gln142=
NM_001330624.1:c.426G=	NP_001317553.1:p.Gln142=
NM_001079872.2:c.411G= MANE Select	NP_001073341.1:p.Gln137=
NM_001330624.2:c.426G=	NP_001317553.1:p.Gln142=
NM_003588.4:c.465G=	NP_003579.3:p.Gln155=