Canonical Allele Identifier: CA983684451
Gene: CCR7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40561643dup , CM000679.2:g.40561643dup GRCh38
NC_000017.10:g.38717895dup , CM000679.1:g.38717895dup GRCh37
NC_000017.9:g.35971421dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000246657.2:c.11-2701dup MANE Select ENSP00000246657.2:n.11-2701dup
ENST00000578085.1:c.-130+3757dup ENSP00000463075.1:n.-130+3757dup
NM_001301714.1:c.-130+3757dup NP_001288643.1:n.-130+3757dup
NM_001838.3:c.11-2701dup NP_001829.1:n.11-2701dup
NM_001838.4:c.11-2701dup MANE Select NP_001829.1:n.11-2701dup
NM_001301714.2:c.-130+3757dup NP_001288643.1:n.-130+3757dup