Canonical Allele Identifier: CA475219577

Gene: CCND1

Linked Data

• MyVariant Identifiers: chr11:g.69462889C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648121C>G , CM000673.2:g.69648121C>G	GRCh38
NC_000011.9:g.69462889C>G , CM000673.1:g.69462889C>G	GRCh37
NC_000011.8:g.69172070C>G	NCBI36
NG_007375.1:g.12017C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.702C>G MANE Select	ENSP00000227507.2:p.Ser234=
ENST00000227507.2:c.702C>G	ENSP00000227507.2:p.Ser234=
ENST00000536559.1:c.*122C>G	ENSP00000438482.1:n.*122C>G
ENST00000542367.1:n.165C>G
ENST00000545484.1:n.408C>G
NM_053056.2:c.702C>G	NP_444284.1:p.Ser234=
XM_006718653.2:c.726C>G	XP_006718716.1:p.Ser242=
NM_053056.3:c.702C>G MANE Select	NP_444284.1:p.Ser234=