Canonical Allele Identifier: CA1543080148
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305482_44305486delinsGTGAT , CM000667.2:g.44305482_44305486delinsGTGAT GRCh38
NC_000005.9:g.44305584_44305588delinsGTGAT , CM000667.1:g.44305584_44305588delinsGTGAT GRCh37
NC_000005.8:g.44341341_44341345delinsGTGAT NCBI36
NG_011446.1:g.88197_88201delinsATCAC

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.430-294_430-290delinsATCAC MANE Select ENSP00000264664.4:n.430-294_430-290delinsATCAC
ENST00000264664.4:c.430-294_430-290delinsATCAC ENSP00000264664.4:n.430-294_430-290delinsATCAC
NM_004465.1:c.430-294_430-290delinsATCAC NP_004456.1:n.430-294_430-290delinsATCAC
XM_005248264.2:c.430-294_430-290delinsATCAC XP_005248321.1:n.430-294_430-290delinsATCAC
XM_005248264.4:c.430-294_430-290delinsATCAC XP_005248321.1:n.430-294_430-290delinsATCAC
NM_004465.2:c.430-294_430-290delinsATCAC MANE Select NP_004456.1:n.430-294_430-290delinsATCAC