Canonical Allele Identifier: CA1543079890
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305284_44305285delinsTC , CM000667.2:g.44305284_44305285delinsTC GRCh38
NC_000005.9:g.44305386_44305387delinsTC , CM000667.1:g.44305386_44305387delinsTC GRCh37
NC_000005.8:g.44341143_44341144delinsTC NCBI36
NG_011446.1:g.88398_88399delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-93_430-92delinsGA MANE Select ENSP00000264664.4:n.430-93_430-92delinsGA
ENST00000264664.4:c.430-93_430-92delinsGA ENSP00000264664.4:n.430-93_430-92delinsGA
NM_004465.1:c.430-93_430-92delinsGA NP_004456.1:n.430-93_430-92delinsGA
XM_005248264.2:c.430-93_430-92delinsGA XP_005248321.1:n.430-93_430-92delinsGA
XM_005248264.4:c.430-93_430-92delinsGA XP_005248321.1:n.430-93_430-92delinsGA
NM_004465.2:c.430-93_430-92delinsGA MANE Select NP_004456.1:n.430-93_430-92delinsGA