Canonical Allele Identifier: CA1543080240
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305549A= , CM000667.2:g.44305549A= GRCh38
NC_000005.9:g.44305651A= , CM000667.1:g.44305651A= GRCh37
NC_000005.8:g.44341408A= NCBI36
NG_011446.1:g.88134T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.430-357T= MANE Select ENSP00000264664.4:n.430-357T=
ENST00000264664.4:c.430-357T= ENSP00000264664.4:n.430-357T=
NM_004465.1:c.430-357T= NP_004456.1:n.430-357T=
XM_005248264.2:c.430-357T= XP_005248321.1:n.430-357T=
XM_005248264.4:c.430-357T= XP_005248321.1:n.430-357T=
NM_004465.2:c.430-357T= MANE Select NP_004456.1:n.430-357T=