Canonical Allele Identifier: CA381657994

Gene: CCND1

Linked Data

• dbSNP Id: rs751664590
• MyVariant Identifiers: chr11:g.69462797G>T (hg19) ; chr11:g.69648029G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648029G>T , CM000673.2:g.69648029G>T	GRCh38
NC_000011.9:g.69462797G>T , CM000673.1:g.69462797G>T	GRCh37
NC_000011.8:g.69171978G>T	NCBI36
NG_007375.1:g.11925G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.610G>T MANE Select	ENSP00000227507.2:p.Ala204Ser
ENST00000227507.2:c.610G>T	ENSP00000227507.2:p.Ala204Ser
ENST00000536559.1:c.*30G>T	ENSP00000438482.1:n.*30G>T
ENST00000542367.1:n.73G>T
ENST00000545484.1:n.316G>T
NM_053056.2:c.610G>T	NP_444284.1:p.Ala204Ser
XM_006718653.2:c.634G>T	XP_006718716.1:p.Ala212Ser
NM_053056.3:c.610G>T MANE Select	NP_444284.1:p.Ala204Ser