Canonical Allele Identifier: CA1543079701
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305160C= , CM000667.2:g.44305160C= GRCh38
NC_000005.9:g.44305262C= , CM000667.1:g.44305262C= GRCh37
NC_000005.8:g.44341019C= NCBI36
NG_011446.1:g.88523G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.462G= MANE Select ENSP00000264664.4:p.Glu154=
ENST00000264664.4:c.462G= ENSP00000264664.4:p.Glu154=
NM_004465.1:c.462G= NP_004456.1:p.Glu154=
XM_005248264.2:c.462G= XP_005248321.1:p.Glu154=
XM_005248264.4:c.462G= XP_005248321.1:p.Glu154=
NM_004465.2:c.462G= MANE Select NP_004456.1:p.Glu154=