Canonical Allele Identifier: CA1075639650
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1740832225
gnomAD v3: 5-44335642-T-TG
gnomAD v4: 5-44335642-T-TG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335644dup , CM000667.2:g.44335644dup GRCh38
NC_000005.9:g.44335746dup , CM000667.1:g.44335746dup GRCh37
NC_000005.8:g.44371503dup NCBI36
NG_011446.1:g.58040dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.326-25113dup MANE Select ENSP00000264664.4:n.326-25113dup
ENST00000264664.4:c.326-25113dup ENSP00000264664.4:n.326-25113dup
NM_004465.1:c.326-25113dup NP_004456.1:n.326-25113dup
XM_005248264.2:c.326-25113dup XP_005248321.1:n.326-25113dup
XM_005248264.4:c.326-25113dup XP_005248321.1:n.326-25113dup
NM_004465.2:c.326-25113dup MANE Select NP_004456.1:n.326-25113dup
Search 100 bp 5'
Search 100 bp 3'