Canonical Allele Identifier: CA2614779932

Gene: CCND1

Linked Data

• gnomAD v4: 11-69647889-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69647889G>T , CM000673.2:g.69647889G>T	GRCh38
NC_000011.9:g.69462657G>T , CM000673.1:g.69462657G>T	GRCh37
NC_000011.8:g.69171838G>T	NCBI36
NG_007375.1:g.11785G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.575-105G>T MANE Select	ENSP00000227507.2:n.575-105G>T
ENST00000227507.2:c.575-105G>T	ENSP00000227507.2:n.575-105G>T
ENST00000536559.1:c.199-105G>T	ENSP00000438482.1:n.199-105G>T
ENST00000545484.1:n.281-105G>T
NM_053056.2:c.575-105G>T	NP_444284.1:n.575-105G>T
XM_006718653.2:c.599-105G>T	XP_006718716.1:n.599-105G>T
NM_053056.3:c.575-105G>T MANE Select	NP_444284.1:n.575-105G>T