Canonical Allele Identifier: CA381657919

Gene: CCND1

Linked Data

• dbSNP Id: rs201012923
• MyVariant Identifiers: chr11:g.69462764G>T (hg19) ; chr11:g.69647996G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69647996G>T , CM000673.2:g.69647996G>T	GRCh38
NC_000011.9:g.69462764G>T , CM000673.1:g.69462764G>T	GRCh37
NC_000011.8:g.69171945G>T	NCBI36
NG_007375.1:g.11892G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.577G>T MANE Select	ENSP00000227507.2:p.Val193Leu
ENST00000227507.2:c.577G>T	ENSP00000227507.2:p.Val193Leu
ENST00000536559.1:c.201G>T	ENSP00000438482.1:p.Met67Ile
ENST00000542367.1:n.40G>T
ENST00000545484.1:n.283G>T
NM_053056.2:c.577G>T	NP_444284.1:p.Val193Leu
XM_006718653.2:c.601G>T	XP_006718716.1:p.Val201Leu
NM_053056.3:c.577G>T MANE Select	NP_444284.1:p.Val193Leu