Canonical Allele Identifier: CA2519900247

Gene: CCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40561471A>G , CM000679.2:g.40561471A>G	GRCh38
NC_000017.10:g.38717723A>G , CM000679.1:g.38717723A>G	GRCh37
NC_000017.9:g.35971249A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000246657.2:c.11-2529T>C MANE Select	ENSP00000246657.2:n.11-2529T>C
ENST00000578085.1:c.-130+3929T>C	ENSP00000463075.1:n.-130+3929T>C
NM_001301714.1:c.-130+3929T>C	NP_001288643.1:n.-130+3929T>C
NM_001838.3:c.11-2529T>C	NP_001829.1:n.11-2529T>C
NM_001838.4:c.11-2529T>C MANE Select	NP_001829.1:n.11-2529T>C
NM_001301714.2:c.-130+3929T>C	NP_001288643.1:n.-130+3929T>C