Canonical Allele Identifier: CA118160613
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs931175610
gnomAD v2: 5-44305826-A-AG
gnomAD v3: 5-44305724-A-AG
gnomAD v4: 5-44305724-A-AG
MyVariant Identifiers: chr5:g.44305826_44305827insG (hg19) chr5:g.44305724_44305725insG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305731dup , CM000667.2:g.44305731dup GRCh38
NC_000005.9:g.44305833dup , CM000667.1:g.44305833dup GRCh37
NC_000005.8:g.44341590dup NCBI36
NG_011446.1:g.87958dup

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.430-533dup MANE Select ENSP00000264664.4:n.430-533dup
ENST00000264664.4:c.430-533dup ENSP00000264664.4:n.430-533dup
NM_004465.1:c.430-533dup NP_004456.1:n.430-533dup
XM_005248264.2:c.430-533dup XP_005248321.1:n.430-533dup
XM_005248264.4:c.430-533dup XP_005248321.1:n.430-533dup
NM_004465.2:c.430-533dup MANE Select NP_004456.1:n.430-533dup
Search 100 bp 5'
Search 100 bp 3'