Canonical Allele Identifier: CA1543079829
Gene: FGF10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305230A= , CM000667.2:g.44305230A= GRCh38
NC_000005.9:g.44305332A= , CM000667.1:g.44305332A= GRCh37
NC_000005.8:g.44341089A= NCBI36
NG_011446.1:g.88453T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-38T= MANE Select ENSP00000264664.4:n.430-38T=
ENST00000264664.4:c.430-38T= ENSP00000264664.4:n.430-38T=
NM_004465.1:c.430-38T= NP_004456.1:n.430-38T=
XM_005248264.2:c.430-38T= XP_005248321.1:n.430-38T=
XM_005248264.4:c.430-38T= XP_005248321.1:n.430-38T=
NM_004465.2:c.430-38T= MANE Select NP_004456.1:n.430-38T=
Search 100 bp 5'
Search 100 bp 3'