Canonical Allele Identifier: CA381657955

Gene: CCND1

Linked Data

• MyVariant Identifiers: chr11:g.69462779A>T (hg19) ; chr11:g.69648011A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648011A>T , CM000673.2:g.69648011A>T	GRCh38
NC_000011.9:g.69462779A>T , CM000673.1:g.69462779A>T	GRCh37
NC_000011.8:g.69171960A>T	NCBI36
NG_007375.1:g.11907A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.592A>T MANE Select	ENSP00000227507.2:p.Asn198Tyr
ENST00000227507.2:c.592A>T	ENSP00000227507.2:p.Asn198Tyr
ENST00000536559.1:c.*12A>T	ENSP00000438482.1:n.*12A>T
ENST00000542367.1:n.55A>T
ENST00000545484.1:n.298A>T
NM_053056.2:c.592A>T	NP_444284.1:p.Asn198Tyr
XM_006718653.2:c.616A>T	XP_006718716.1:p.Asn206Tyr
NM_053056.3:c.592A>T MANE Select	NP_444284.1:p.Asn198Tyr