Canonical Allele Identifier: CA1543087698
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335639T= , CM000667.2:g.44335639T= GRCh38
NC_000005.9:g.44335741T= , CM000667.1:g.44335741T= GRCh37
NC_000005.8:g.44371498T= NCBI36
NG_011446.1:g.58044A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.326-25109A= MANE Select ENSP00000264664.4:n.326-25109A=
ENST00000264664.4:c.326-25109A= ENSP00000264664.4:n.326-25109A=
NM_004465.1:c.326-25109A= NP_004456.1:n.326-25109A=
XM_005248264.2:c.326-25109A= XP_005248321.1:n.326-25109A=
XM_005248264.4:c.326-25109A= XP_005248321.1:n.326-25109A=
NM_004465.2:c.326-25109A= MANE Select NP_004456.1:n.326-25109A=