Canonical Allele Identifier: CA1543087671
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1740831676

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335622dup , CM000667.2:g.44335622dup GRCh38
NC_000005.9:g.44335724dup , CM000667.1:g.44335724dup GRCh37
NC_000005.8:g.44371481dup NCBI36
NG_011446.1:g.58066dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.326-25087dup MANE Select ENSP00000264664.4:n.326-25087dup
ENST00000264664.4:c.326-25087dup ENSP00000264664.4:n.326-25087dup
NM_004465.1:c.326-25087dup NP_004456.1:n.326-25087dup
XM_005248264.2:c.326-25087dup XP_005248321.1:n.326-25087dup
XM_005248264.4:c.326-25087dup XP_005248321.1:n.326-25087dup
NM_004465.2:c.326-25087dup MANE Select NP_004456.1:n.326-25087dup