Canonical Allele Identifier: CA1397784330
Gene: CD86 HGNC NCBI

Linked Data

dbSNP Id: rs2072418177
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122066737_122066738insAGGCTAT , CM000665.2:g.122066737_122066738insAGGCTAT GRCh38
NC_000003.11:g.121785584_121785585insAGGCTAT , CM000665.1:g.121785584_121785585insAGGCTAT GRCh37
NC_000003.10:g.123268274_123268275insAGGCTAT NCBI36
NG_029928.1:g.16376_16377insAGGCTAT

Transcript Alleles

HGVS Amino-acid change
ENST00000330540.7:c.14+11234_14+11235insAGGCTAT MANE Select ENSP00000332049.2:n.14+11234_14+11235insA...
ENST00000330540.6:c.14+11234_14+11235insAGGCTAT ENSP00000332049.2:n.14+11234_14+11235insA...
ENST00000469710.5:c.-183+11234_-183+11235insAGGCTAT ENSP00000418988.1:n.-183+11234_-183+11235...
ENST00000478390.1:n.127+11234_127+11235insAGGCTAT
ENST00000493101.5:c.14+11234_14+11235insAGGCTAT ENSP00000420230.1:n.14+11234_14+11235insA...
NM_001206924.1:c.14+11234_14+11235insAGGCTAT NP_001193853.1:n.14+11234_14+11235insAGGC...
NM_001206925.1:c.-183+11234_-183+11235insAGGCTAT NP_001193854.1:n.-183+11234_-183+11235ins...
NM_175862.4:c.14+11234_14+11235insAGGCTAT NP_787058.4:n.14+11234_14+11235insAGGCTAT...
NM_175862.5:c.14+11234_14+11235insAGGCTAT MANE Select NP_787058.5:n.14+11234_14+11235insAGGCTAT...
NM_001206924.2:c.14+11234_14+11235insAGGCTAT NP_001193853.2:n.14+11234_14+11235insAGGC...
NM_001206925.2:c.-183+11234_-183+11235insAGGCTAT NP_001193854.2:n.-183+11234_-183+11235ins...
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