Canonical Allele Identifier: CA1543080648
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305788_44305789delinsTA , CM000667.2:g.44305788_44305789delinsTA GRCh38
NC_000005.9:g.44305890_44305891delinsTA , CM000667.1:g.44305890_44305891delinsTA GRCh37
NC_000005.8:g.44341647_44341648delinsTA NCBI36
NG_011446.1:g.87894_87895delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-597_430-596delinsTA MANE Select ENSP00000264664.4:n.430-597_430-596delinsTA
ENST00000264664.4:c.430-597_430-596delinsTA ENSP00000264664.4:n.430-597_430-596delinsTA
NM_004465.1:c.430-597_430-596delinsTA NP_004456.1:n.430-597_430-596delinsTA
XM_005248264.2:c.430-597_430-596delinsTA XP_005248321.1:n.430-597_430-596delinsTA
XM_005248264.4:c.430-597_430-596delinsTA XP_005248321.1:n.430-597_430-596delinsTA
NM_004465.2:c.430-597_430-596delinsTA MANE Select NP_004456.1:n.430-597_430-596delinsTA