Canonical Allele Identifier: CA2505695199

Gene: CCND1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69650086C>T , CM000673.2:g.69650086C>T	GRCh38
NC_000011.9:g.69464854C>T , CM000673.1:g.69464854C>T	GRCh37
NC_000011.8:g.69174035C>T	NCBI36
NG_007375.1:g.13982C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.724-1032C>T MANE Select	ENSP00000227507.2:n.724-1032C>T
ENST00000227507.2:c.724-1032C>T	ENSP00000227507.2:n.724-1032C>T
ENST00000542367.1:n.187-1032C>T
NM_053056.2:c.724-1032C>T	NP_444284.1:n.724-1032C>T
XM_006718653.2:c.748-1032C>T	XP_006718716.1:n.748-1032C>T
NM_053056.3:c.724-1032C>T MANE Select	NP_444284.1:n.724-1032C>T