Canonical Allele Identifier: CA381657927

Gene: CCND1

Linked Data

• MyVariant Identifiers: chr11:g.69462767A>G (hg19) ; chr11:g.69647999A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69647999A>G , CM000673.2:g.69647999A>G	GRCh38
NC_000011.9:g.69462767A>G , CM000673.1:g.69462767A>G	GRCh37
NC_000011.8:g.69171948A>G	NCBI36
NG_007375.1:g.11895A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.580A>G MANE Select	ENSP00000227507.2:p.Lys194Glu
ENST00000227507.2:c.580A>G	ENSP00000227507.2:p.Lys194Glu
ENST00000536559.1:c.204A>G	ENSP00000438482.1:p.Ter68Trp
ENST00000542367.1:n.43A>G
ENST00000545484.1:n.286A>G
NM_053056.2:c.580A>G	NP_444284.1:p.Lys194Glu
XM_006718653.2:c.604A>G	XP_006718716.1:p.Lys202Glu
NM_053056.3:c.580A>G MANE Select	NP_444284.1:p.Lys194Glu