Canonical Allele Identifier: CA2581481655
Gene: FGF10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305207C>T , CM000667.2:g.44305207C>T GRCh38
NC_000005.9:g.44305309C>T , CM000667.1:g.44305309C>T GRCh37
NC_000005.8:g.44341066C>T NCBI36
NG_011446.1:g.88476G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-15G>A MANE Select ENSP00000264664.4:n.430-15G>A
ENST00000264664.4:c.430-15G>A ENSP00000264664.4:n.430-15G>A
NM_004465.1:c.430-15G>A NP_004456.1:n.430-15G>A
XM_005248264.2:c.430-15G>A XP_005248321.1:n.430-15G>A
XM_005248264.4:c.430-15G>A XP_005248321.1:n.430-15G>A
NM_004465.2:c.430-15G>A MANE Select NP_004456.1:n.430-15G>A
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