Canonical Allele Identifier: CA381658108

Gene: CCND1

Linked Data

• dbSNP Id: rs2120109482
• MyVariant Identifiers: chr11:g.69462852A>T (hg19) ; chr11:g.69648084A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648084A>T , CM000673.2:g.69648084A>T	GRCh38
NC_000011.9:g.69462852A>T , CM000673.1:g.69462852A>T	GRCh37
NC_000011.8:g.69172033A>T	NCBI36
NG_007375.1:g.11980A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.665A>T MANE Select	ENSP00000227507.2:p.Asn222Ile
ENST00000227507.2:c.665A>T	ENSP00000227507.2:p.Asn222Ile
ENST00000536559.1:c.*85A>T	ENSP00000438482.1:n.*85A>T
ENST00000542367.1:n.128A>T
ENST00000545484.1:n.371A>T
NM_053056.2:c.665A>T	NP_444284.1:p.Asn222Ile
XM_006718653.2:c.689A>T	XP_006718716.1:p.Asn230Ile
NM_053056.3:c.665A>T MANE Select	NP_444284.1:p.Asn222Ile