Canonical Allele Identifier: CA475219539

Gene: CCND1

Linked Data

• MyVariant Identifiers: chr11:g.69462830C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648062C>T , CM000673.2:g.69648062C>T	GRCh38
NC_000011.9:g.69462830C>T , CM000673.1:g.69462830C>T	GRCh37
NC_000011.8:g.69172011C>T	NCBI36
NG_007375.1:g.11958C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.643C>T MANE Select	ENSP00000227507.2:p.Leu215=
ENST00000227507.2:c.643C>T	ENSP00000227507.2:p.Leu215=
ENST00000536559.1:c.*63C>T	ENSP00000438482.1:n.*63C>T
ENST00000542367.1:n.106C>T
ENST00000545484.1:n.349C>T
NM_053056.2:c.643C>T	NP_444284.1:p.Leu215=
XM_006718653.2:c.667C>T	XP_006718716.1:p.Leu223=
NM_053056.3:c.643C>T MANE Select	NP_444284.1:p.Leu215=