Canonical Allele Identifier: CA1543088042
Gene: FGF10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335821C= , CM000667.2:g.44335821C= GRCh38
NC_000005.9:g.44335923C= , CM000667.1:g.44335923C= GRCh37
NC_000005.8:g.44371680C= NCBI36
NG_011446.1:g.57862G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.326-25291G= MANE Select ENSP00000264664.4:n.326-25291G=
ENST00000264664.4:c.326-25291G= ENSP00000264664.4:n.326-25291G=
NM_004465.1:c.326-25291G= NP_004456.1:n.326-25291G=
XM_005248264.2:c.326-25291G= XP_005248321.1:n.326-25291G=
XM_005248264.4:c.326-25291G= XP_005248321.1:n.326-25291G=
NM_004465.2:c.326-25291G= MANE Select NP_004456.1:n.326-25291G=
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