Canonical Allele Identifier: CA118874
Community Standard Title: NM_004465.2(FGF10):c.413G>A (p.Gly138Glu)
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44310443C>T , CM000667.2:g.44310443C>T GRCh38
NC_000005.9:g.44310545C>T , CM000667.1:g.44310545C>T GRCh37
NC_000005.8:g.44346302C>T NCBI36
NG_011446.1:g.83240G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004465.2:c.413G>A MANE Select NP_004456.1:p.Gly138Glu
ENST00000264664.5:c.413G>A MANE Select ENSP00000264664.4:p.Gly138Glu
NM_004465.1:c.413G>A NP_004456.1:p.Gly138Glu
ENST00000264664.4:c.413G>A ENSP00000264664.4:p.Gly138Glu
XM_005248264.2:c.413G>A XP_005248321.1:p.Gly138Glu
XM_005248264.4:c.413G>A XP_005248321.1:p.Gly138Glu