Canonical Allele Identifier: CA475219517

Gene: CCND1

Linked Data

• dbSNP Id: rs761742200
• COSMIC: COSM382780
• MyVariant Identifiers: chr11:g.69462802G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648034G>T , CM000673.2:g.69648034G>T	GRCh38
NC_000011.9:g.69462802G>T , CM000673.1:g.69462802G>T	GRCh37
NC_000011.8:g.69171983G>T	NCBI36
NG_007375.1:g.11930G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.615G>T MANE Select	ENSP00000227507.2:p.Ala205=
ENST00000227507.2:c.615G>T	ENSP00000227507.2:p.Ala205=
ENST00000536559.1:c.*35G>T	ENSP00000438482.1:n.*35G>T
ENST00000542367.1:n.78G>T
ENST00000545484.1:n.321G>T
NM_053056.2:c.615G>T	NP_444284.1:p.Ala205=
XM_006718653.2:c.639G>T	XP_006718716.1:p.Ala213=
NM_053056.3:c.615G>T MANE Select	NP_444284.1:p.Ala205=