Canonical Allele Identifier: CA381657999
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1193747086
gnomAD v2: 11-69462800-G-T
gnomAD v4: 11-69648032-G-T
COSMIC: COSM4382987 COSM4382988
MyVariant Identifiers: chr11:g.69462800G>T (hg19) chr11:g.69648032G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648032G>T , CM000673.2:g.69648032G>T GRCh38
NC_000011.9:g.69462800G>T , CM000673.1:g.69462800G>T GRCh37
NC_000011.8:g.69171981G>T NCBI36
NG_007375.1:g.11928G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.613G>T MANE Select ENSP00000227507.2:p.Ala205Ser
ENST00000227507.2:c.613G>T ENSP00000227507.2:p.Ala205Ser
ENST00000536559.1:c.*33G>T ENSP00000438482.1:n.*33G>T
ENST00000542367.1:n.76G>T
ENST00000545484.1:n.319G>T
NM_053056.2:c.613G>T NP_444284.1:p.Ala205Ser
XM_006718653.2:c.637G>T XP_006718716.1:p.Ala213Ser
NM_053056.3:c.613G>T MANE Select NP_444284.1:p.Ala205Ser
Search 100 bp 5'
Search 100 bp 3'