Canonical Allele Identifier: CA2518403273
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44375118_44375119insGG , CM000667.2:g.44375118_44375119insGG GRCh38
NC_000005.9:g.44375220_44375221insGG , CM000667.1:g.44375220_44375221insGG GRCh37
NC_000005.8:g.44410977_44410978insGG NCBI36
NG_011446.1:g.18564_18565insCC

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+13239_325+13240insCC MANE Select ENSP00000264664.4:n.325+13239_325+13240in...
ENST00000264664.4:c.325+13239_325+13240insCC ENSP00000264664.4:n.325+13239_325+13240in...
NM_004465.1:c.325+13239_325+13240insCC NP_004456.1:n.325+13239_325+13240insCC
XM_005248264.2:c.325+13239_325+13240insCC XP_005248321.1:n.325+13239_325+13240insCC...
XM_005248264.4:c.325+13239_325+13240insCC XP_005248321.1:n.325+13239_325+13240insCC...
NM_004465.2:c.325+13239_325+13240insCC MANE Select NP_004456.1:n.325+13239_325+13240insCC