Canonical Allele Identifier: CA381658122
Gene: CCND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.69462858T>G (hg19) chr11:g.69648090T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648090T>G , CM000673.2:g.69648090T>G GRCh38
NC_000011.9:g.69462858T>G , CM000673.1:g.69462858T>G GRCh37
NC_000011.8:g.69172039T>G NCBI36
NG_007375.1:g.11986T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.671T>G MANE Select ENSP00000227507.2:p.Leu224Arg
ENST00000227507.2:c.671T>G ENSP00000227507.2:p.Leu224Arg
ENST00000536559.1:c.*91T>G ENSP00000438482.1:n.*91T>G
ENST00000542367.1:n.134T>G
ENST00000545484.1:n.377T>G
NM_053056.2:c.671T>G NP_444284.1:p.Leu224Arg
XM_006718653.2:c.695T>G XP_006718716.1:p.Leu232Arg
NM_053056.3:c.671T>G MANE Select NP_444284.1:p.Leu224Arg
Search 100 bp 5'
Search 100 bp 3'