Canonical Allele Identifier: CA1543090626
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388366C= , CM000667.2:g.44388366C= GRCh38
NC_000005.9:g.44388468C= , CM000667.1:g.44388468C= GRCh37
NC_000005.8:g.44424225C= NCBI36
NG_011446.1:g.5317G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.317G= MANE Select ENSP00000264664.4:p.Cys106=
ENST00000264664.4:c.317G= ENSP00000264664.4:p.Cys106=
NM_004465.1:c.317G= NP_004456.1:p.Cys106=
XM_005248264.2:c.317G= XP_005248321.1:p.Cys106=
XM_005248264.4:c.317G= XP_005248321.1:p.Cys106=
NM_004465.2:c.317G= MANE Select NP_004456.1:p.Cys106=