Canonical Allele Identifier: CA1543080476
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305695C= , CM000667.2:g.44305695C= GRCh38
NC_000005.9:g.44305797C= , CM000667.1:g.44305797C= GRCh37
NC_000005.8:g.44341554C= NCBI36
NG_011446.1:g.87988G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.430-503G= MANE Select ENSP00000264664.4:n.430-503G=
ENST00000264664.4:c.430-503G= ENSP00000264664.4:n.430-503G=
NM_004465.1:c.430-503G= NP_004456.1:n.430-503G=
XM_005248264.2:c.430-503G= XP_005248321.1:n.430-503G=
XM_005248264.4:c.430-503G= XP_005248321.1:n.430-503G=
NM_004465.2:c.430-503G= MANE Select NP_004456.1:n.430-503G=