Canonical Allele Identifier: CA1543080283
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305572A= , CM000667.2:g.44305572A= GRCh38
NC_000005.9:g.44305674A= , CM000667.1:g.44305674A= GRCh37
NC_000005.8:g.44341431A= NCBI36
NG_011446.1:g.88111T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-380T= MANE Select ENSP00000264664.4:n.430-380T=
ENST00000264664.4:c.430-380T= ENSP00000264664.4:n.430-380T=
NM_004465.1:c.430-380T= NP_004456.1:n.430-380T=
XM_005248264.2:c.430-380T= XP_005248321.1:n.430-380T=
XM_005248264.4:c.430-380T= XP_005248321.1:n.430-380T=
NM_004465.2:c.430-380T= MANE Select NP_004456.1:n.430-380T=