Canonical Allele Identifier: CA1543129016
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365517A= , CM000667.2:g.44365517A= GRCh38
NC_000005.9:g.44365619A= , CM000667.1:g.44365619A= GRCh37
NC_000005.8:g.44401376A= NCBI36
NG_011446.1:g.28166T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.325+22841T= MANE Select ENSP00000264664.4:n.325+22841T=
ENST00000264664.4:c.325+22841T= ENSP00000264664.4:n.325+22841T=
NM_004465.1:c.325+22841T= NP_004456.1:n.325+22841T=
XM_005248264.2:c.325+22841T= XP_005248321.1:n.325+22841T=
XM_005248264.4:c.325+22841T= XP_005248321.1:n.325+22841T=
NM_004465.2:c.325+22841T= MANE Select NP_004456.1:n.325+22841T=