Canonical Allele Identifier: CA2614780058

Gene: CCND1

Linked Data

• gnomAD v4: 11-69648249-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648249G>T , CM000673.2:g.69648249G>T	GRCh38
NC_000011.9:g.69463017G>T , CM000673.1:g.69463017G>T	GRCh37
NC_000011.8:g.69172198G>T	NCBI36
NG_007375.1:g.12145G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723+107G>T MANE Select	ENSP00000227507.2:n.723+107G>T
ENST00000227507.2:c.723+107G>T	ENSP00000227507.2:n.723+107G>T
ENST00000542367.1:n.186+107G>T
NM_053056.2:c.723+107G>T	NP_444284.1:n.723+107G>T
XM_006718653.2:c.747+107G>T	XP_006718716.1:n.747+107G>T
NM_053056.3:c.723+107G>T MANE Select	NP_444284.1:n.723+107G>T