Canonical Allele Identifier: CA1543087779
Gene: FGF10 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335675G= , CM000667.2:g.44335675G= GRCh38
NC_000005.9:g.44335777G= , CM000667.1:g.44335777G= GRCh37
NC_000005.8:g.44371534G= NCBI36
NG_011446.1:g.58008C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.326-25145C= MANE Select ENSP00000264664.4:n.326-25145C=
ENST00000264664.4:c.326-25145C= ENSP00000264664.4:n.326-25145C=
NM_004465.1:c.326-25145C= NP_004456.1:n.326-25145C=
XM_005248264.2:c.326-25145C= XP_005248321.1:n.326-25145C=
XM_005248264.4:c.326-25145C= XP_005248321.1:n.326-25145C=
NM_004465.2:c.326-25145C= MANE Select NP_004456.1:n.326-25145C=
Search 100 bp 5'
Search 100 bp 3'