Canonical Allele Identifier: CA1543080267
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305566G= , CM000667.2:g.44305566G= GRCh38
NC_000005.9:g.44305668G= , CM000667.1:g.44305668G= GRCh37
NC_000005.8:g.44341425G= NCBI36
NG_011446.1:g.88117C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.430-374C= MANE Select ENSP00000264664.4:n.430-374C=
ENST00000264664.4:c.430-374C= ENSP00000264664.4:n.430-374C=
NM_004465.1:c.430-374C= NP_004456.1:n.430-374C=
XM_005248264.2:c.430-374C= XP_005248321.1:n.430-374C=
XM_005248264.4:c.430-374C= XP_005248321.1:n.430-374C=
NM_004465.2:c.430-374C= MANE Select NP_004456.1:n.430-374C=