Canonical Allele Identifier: CA1543124786
Gene: FGF10 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44359475A= , CM000667.2:g.44359475A= GRCh38
NC_000005.9:g.44359577A= , CM000667.1:g.44359577A= GRCh37
NC_000005.8:g.44395334A= NCBI36
NG_011446.1:g.34208T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.325+28883T= MANE Select ENSP00000264664.4:n.325+28883T=
ENST00000264664.4:c.325+28883T= ENSP00000264664.4:n.325+28883T=
NM_004465.1:c.325+28883T= NP_004456.1:n.325+28883T=
XM_005248264.2:c.325+28883T= XP_005248321.1:n.325+28883T=
XM_005248264.4:c.325+28883T= XP_005248321.1:n.325+28883T=
NM_004465.2:c.325+28883T= MANE Select NP_004456.1:n.325+28883T=
Search 100 bp 5'
Search 100 bp 3'