Canonical Allele Identifier: CA1543124707
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44359363G= , CM000667.2:g.44359363G= GRCh38
NC_000005.9:g.44359465G= , CM000667.1:g.44359465G= GRCh37
NC_000005.8:g.44395222G= NCBI36
NG_011446.1:g.34320C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+28995C= MANE Select ENSP00000264664.4:n.325+28995C=
ENST00000264664.4:c.325+28995C= ENSP00000264664.4:n.325+28995C=
NM_004465.1:c.325+28995C= NP_004456.1:n.325+28995C=
XM_005248264.2:c.325+28995C= XP_005248321.1:n.325+28995C=
XM_005248264.4:c.325+28995C= XP_005248321.1:n.325+28995C=
NM_004465.2:c.325+28995C= MANE Select NP_004456.1:n.325+28995C=