Canonical Allele Identifier: CA1543088047
Gene: FGF10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335826T= , CM000667.2:g.44335826T= GRCh38
NC_000005.9:g.44335928T= , CM000667.1:g.44335928T= GRCh37
NC_000005.8:g.44371685T= NCBI36
NG_011446.1:g.57857A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.326-25296A= MANE Select ENSP00000264664.4:n.326-25296A=
ENST00000264664.4:c.326-25296A= ENSP00000264664.4:n.326-25296A=
NM_004465.1:c.326-25296A= NP_004456.1:n.326-25296A=
XM_005248264.2:c.326-25296A= XP_005248321.1:n.326-25296A=
XM_005248264.4:c.326-25296A= XP_005248321.1:n.326-25296A=
NM_004465.2:c.326-25296A= MANE Select NP_004456.1:n.326-25296A=
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