Canonical Allele Identifier: CA1543090647
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388372T= , CM000667.2:g.44388372T= GRCh38
NC_000005.9:g.44388474T= , CM000667.1:g.44388474T= GRCh37
NC_000005.8:g.44424231T= NCBI36
NG_011446.1:g.5311A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.311A= MANE Select ENSP00000264664.4:p.Glu104=
ENST00000264664.4:c.311A= ENSP00000264664.4:p.Glu104=
NM_004465.1:c.311A= NP_004456.1:p.Glu104=
XM_005248264.2:c.311A= XP_005248321.1:p.Glu104=
XM_005248264.4:c.311A= XP_005248321.1:p.Glu104=
NM_004465.2:c.311A= MANE Select NP_004456.1:p.Glu104=