Canonical Allele Identifier: CA223474760
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs961056734
gnomAD v2: 11-69463018-T-TTGGGGC
gnomAD v3: 11-69648250-T-TTGGGGC
gnomAD v4: 11-69648250-T-TTGGGGC
MyVariant Identifiers: chr11:g.69463018_69463019insTGGGGC (hg19) chr11:g.69648250_69648251insTGGGGC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648261_69648266dup , CM000673.2:g.69648261_69648266dup GRCh38
NC_000011.9:g.69463029_69463034dup , CM000673.1:g.69463029_69463034dup GRCh37
NC_000011.8:g.69172210_69172215dup NCBI36
NG_007375.1:g.12157_12162dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.723+119_723+124dup MANE Select ENSP00000227507.2:n.723+119_723+124dup
ENST00000227507.2:c.723+119_723+124dup ENSP00000227507.2:n.723+119_723+124dup
ENST00000542367.1:n.186+119_186+124dup
NM_053056.2:c.723+119_723+124dup NP_444284.1:n.723+119_723+124dup
XM_006718653.2:c.747+119_747+124dup XP_006718716.1:n.747+119_747+124dup
NM_053056.3:c.723+119_723+124dup MANE Select NP_444284.1:n.723+119_723+124dup
Search 100 bp 5'
Search 100 bp 3'