Canonical Allele Identifier: CA2614779826

Gene: CCND1

Linked Data

• gnomAD v4: 11-69647818-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69647818A>T , CM000673.2:g.69647818A>T	GRCh38
NC_000011.9:g.69462586A>T , CM000673.1:g.69462586A>T	GRCh37
NC_000011.8:g.69171767A>T	NCBI36
NG_007375.1:g.11714A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.575-176A>T MANE Select	ENSP00000227507.2:n.575-176A>T
ENST00000227507.2:c.575-176A>T	ENSP00000227507.2:n.575-176A>T
ENST00000536559.1:c.199-176A>T	ENSP00000438482.1:n.199-176A>T
ENST00000545484.1:n.281-176A>T
NM_053056.2:c.575-176A>T	NP_444284.1:n.575-176A>T
XM_006718653.2:c.599-176A>T	XP_006718716.1:n.599-176A>T
NM_053056.3:c.575-176A>T MANE Select	NP_444284.1:n.575-176A>T