Canonical Allele Identifier: CA2673772738
Gene: FGF10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305210_44305211insTT , CM000667.2:g.44305210_44305211insTT GRCh38
NC_000005.9:g.44305312_44305313insTT , CM000667.1:g.44305312_44305313insTT GRCh37
NC_000005.8:g.44341069_44341070insTT NCBI36
NG_011446.1:g.88472_88473insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-19_430-18insAA MANE Select ENSP00000264664.4:n.430-19_430-18insAA
ENST00000264664.4:c.430-19_430-18insAA ENSP00000264664.4:n.430-19_430-18insAA
NM_004465.1:c.430-19_430-18insAA NP_004456.1:n.430-19_430-18insAA
XM_005248264.2:c.430-19_430-18insAA XP_005248321.1:n.430-19_430-18insAA
XM_005248264.4:c.430-19_430-18insAA XP_005248321.1:n.430-19_430-18insAA
NM_004465.2:c.430-19_430-18insAA MANE Select NP_004456.1:n.430-19_430-18insAA