Canonical Allele Identifier: CA2574937235

Gene: CCND1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648240G>A , CM000673.2:g.69648240G>A	GRCh38
NC_000011.9:g.69463008G>A , CM000673.1:g.69463008G>A	GRCh37
NC_000011.8:g.69172189G>A	NCBI36
NG_007375.1:g.12136G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723+98G>A MANE Select	ENSP00000227507.2:n.723+98G>A
ENST00000227507.2:c.723+98G>A	ENSP00000227507.2:n.723+98G>A
ENST00000536559.1:c.*241G>A	ENSP00000438482.1:n.*241G>A
ENST00000542367.1:n.186+98G>A
NM_053056.2:c.723+98G>A	NP_444284.1:n.723+98G>A
XM_006718653.2:c.747+98G>A	XP_006718716.1:n.747+98G>A
NM_053056.3:c.723+98G>A MANE Select	NP_444284.1:n.723+98G>A