Canonical Allele Identifier: CA2614779919

Gene: CCND1

Linked Data

• gnomAD v4: 11-69647877-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69647877_69647878insA , CM000673.2:g.69647877_69647878insA	GRCh38
NC_000011.9:g.69462645_69462646insA , CM000673.1:g.69462645_69462646insA	GRCh37
NC_000011.8:g.69171826_69171827insA	NCBI36
NG_007375.1:g.11773_11774insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.575-117_575-116insA MANE Select	ENSP00000227507.2:n.575-117_575-116insA
ENST00000227507.2:c.575-117_575-116insA	ENSP00000227507.2:n.575-117_575-116insA
ENST00000536559.1:c.199-117_199-116insA	ENSP00000438482.1:n.199-117_199-116insA
ENST00000545484.1:n.281-117_281-116insA
NM_053056.2:c.575-117_575-116insA	NP_444284.1:n.575-117_575-116insA
XM_006718653.2:c.599-117_599-116insA	XP_006718716.1:n.599-117_599-116insA
NM_053056.3:c.575-117_575-116insA MANE Select	NP_444284.1:n.575-117_575-116insA