Canonical Allele Identifier: CA2510059863
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305206_44305208dup , CM000667.2:g.44305206_44305208dup GRCh38
NC_000005.9:g.44305308_44305310dup , CM000667.1:g.44305308_44305310dup GRCh37
NC_000005.8:g.44341065_44341067dup NCBI36
NG_011446.1:g.88476_88478dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-15_430-13dup MANE Select ENSP00000264664.4:n.430-15_430-13dup
ENST00000264664.4:c.430-15_430-13dup ENSP00000264664.4:n.430-15_430-13dup
NM_004465.1:c.430-15_430-13dup NP_004456.1:n.430-15_430-13dup
XM_005248264.2:c.430-15_430-13dup XP_005248321.1:n.430-15_430-13dup
XM_005248264.4:c.430-15_430-13dup XP_005248321.1:n.430-15_430-13dup
NM_004465.2:c.430-15_430-13dup MANE Select NP_004456.1:n.430-15_430-13dup