Canonical Allele Identifier: CA2766094469
Gene: FGF10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335697G>A , CM000667.2:g.44335697G>A GRCh38
NC_000005.9:g.44335799G>A , CM000667.1:g.44335799G>A GRCh37
NC_000005.8:g.44371556G>A NCBI36
NG_011446.1:g.57986C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.326-25167C>T MANE Select ENSP00000264664.4:n.326-25167C>T
ENST00000264664.4:c.326-25167C>T ENSP00000264664.4:n.326-25167C>T
NM_004465.1:c.326-25167C>T NP_004456.1:n.326-25167C>T
XM_005248264.2:c.326-25167C>T XP_005248321.1:n.326-25167C>T
XM_005248264.4:c.326-25167C>T XP_005248321.1:n.326-25167C>T
NM_004465.2:c.326-25167C>T MANE Select NP_004456.1:n.326-25167C>T
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