Canonical Allele Identifier: CA359698972
Gene: FGF10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388364G>T , CM000667.2:g.44388364G>T GRCh38
NC_000005.9:g.44388466G>T , CM000667.1:g.44388466G>T GRCh37
NC_000005.8:g.44424223G>T NCBI36
NG_011446.1:g.5319C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.319C>A MANE Select ENSP00000264664.4:p.Pro107Thr
ENST00000264664.4:c.319C>A ENSP00000264664.4:p.Pro107Thr
NM_004465.1:c.319C>A NP_004456.1:p.Pro107Thr
XM_005248264.2:c.319C>A XP_005248321.1:p.Pro107Thr
XM_005248264.4:c.319C>A XP_005248321.1:p.Pro107Thr
NM_004465.2:c.319C>A MANE Select NP_004456.1:p.Pro107Thr