Canonical Allele Identifier: CA1543080639
Gene: FGF10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305786T= , CM000667.2:g.44305786T= GRCh38
NC_000005.9:g.44305888T= , CM000667.1:g.44305888T= GRCh37
NC_000005.8:g.44341645T= NCBI36
NG_011446.1:g.87897A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-594A= MANE Select ENSP00000264664.4:n.430-594A=
ENST00000264664.4:c.430-594A= ENSP00000264664.4:n.430-594A=
NM_004465.1:c.430-594A= NP_004456.1:n.430-594A=
XM_005248264.2:c.430-594A= XP_005248321.1:n.430-594A=
XM_005248264.4:c.430-594A= XP_005248321.1:n.430-594A=
NM_004465.2:c.430-594A= MANE Select NP_004456.1:n.430-594A=
Search 100 bp 5'
Search 100 bp 3'