Canonical Allele Identifier: CA810983641
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1214195510
gnomAD v3: 5-44335836-C-CT
gnomAD v4: 5-44335836-C-CT
MyVariant Identifiers: chr5:g.44335938_44335939insT (hg19) chr5:g.44335836_44335837insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335836_44335837insT , CM000667.2:g.44335836_44335837insT GRCh38
NC_000005.9:g.44335938_44335939insT , CM000667.1:g.44335938_44335939insT GRCh37
NC_000005.8:g.44371695_44371696insT NCBI36
NG_011446.1:g.57846_57847insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.326-25307_326-25306insA MANE Select ENSP00000264664.4:n.326-25307_326-25306insA
ENST00000264664.4:c.326-25307_326-25306insA ENSP00000264664.4:n.326-25307_326-25306insA
NM_004465.1:c.326-25307_326-25306insA NP_004456.1:n.326-25307_326-25306insA
XM_005248264.2:c.326-25307_326-25306insA XP_005248321.1:n.326-25307_326-25306insA
XM_005248264.4:c.326-25307_326-25306insA XP_005248321.1:n.326-25307_326-25306insA
NM_004465.2:c.326-25307_326-25306insA MANE Select NP_004456.1:n.326-25307_326-25306insA
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