Canonical Allele Identifier: CA566942675
Gene: ADGRF4 HGNC NCBI

Linked Data

dbSNP Id: rs1217416149
gnomAD v2: 6-47678136-T-TA
gnomAD v3: 6-47710400-T-TA
gnomAD v4: 6-47710400-T-TA
MyVariant Identifiers: chr6:g.47678136_47678137insA (hg19) chr6:g.47710400_47710401insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.47710402dup , CM000668.2:g.47710402dup GRCh38
NC_000006.11:g.47678138dup , CM000668.1:g.47678138dup GRCh37
NC_000006.10:g.47786097dup NCBI36
NG_052799.1:g.29539dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000283303.3:c.149-333dup MANE Select ENSP00000283303.2:n.149-333dup
ENST00000283303.2:c.149-333dup ENSP00000283303.2:n.149-333dup
ENST00000327753.7:c.149-333dup ENSP00000328319.3:n.149-333dup
ENST00000371220.5:c.320-333dup ENSP00000360264.1:n.320-333dup
NM_153838.3:c.149-333dup NP_722580.3:n.149-333dup
NM_001347855.1:c.149-333dup NP_001334784.1:n.149-333dup
NM_153838.4:c.149-333dup NP_722580.3:n.149-333dup
NM_001347855.2:c.149-333dup NP_001334784.1:n.149-333dup
NM_153838.5:c.149-333dup MANE Select NP_722580.3:n.149-333dup
Search 100 bp 5'
Search 100 bp 3'