Canonical Allele Identifier: CA1543087681
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335620T= , CM000667.2:g.44335620T= GRCh38
NC_000005.9:g.44335722T= , CM000667.1:g.44335722T= GRCh37
NC_000005.8:g.44371479T= NCBI36
NG_011446.1:g.58063A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.326-25090A= MANE Select ENSP00000264664.4:n.326-25090A=
ENST00000264664.4:c.326-25090A= ENSP00000264664.4:n.326-25090A=
NM_004465.1:c.326-25090A= NP_004456.1:n.326-25090A=
XM_005248264.2:c.326-25090A= XP_005248321.1:n.326-25090A=
XM_005248264.4:c.326-25090A= XP_005248321.1:n.326-25090A=
NM_004465.2:c.326-25090A= MANE Select NP_004456.1:n.326-25090A=