Canonical Allele Identifier: CA475219587

Gene: CCND1

Linked Data

• MyVariant Identifiers: chr11:g.69462910G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648142G>T , CM000673.2:g.69648142G>T	GRCh38
NC_000011.9:g.69462910G>T , CM000673.1:g.69462910G>T	GRCh37
NC_000011.8:g.69172091G>T	NCBI36
NG_007375.1:g.12038G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723G>T MANE Select	ENSP00000227507.2:p.Pro241=
ENST00000227507.2:c.723G>T	ENSP00000227507.2:p.Pro241=
ENST00000536559.1:c.*143G>T	ENSP00000438482.1:n.*143G>T
ENST00000542367.1:n.186G>T
ENST00000545484.1:n.429G>T
NM_053056.2:c.723G>T	NP_444284.1:p.Pro241=
XM_006718653.2:c.747G>T	XP_006718716.1:p.Pro249=
NM_053056.3:c.723G>T MANE Select	NP_444284.1:p.Pro241=