Canonical Allele Identifier: CA1075631932
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1741423034

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44359330_44359336del , CM000667.2:g.44359330_44359336del GRCh38
NC_000005.9:g.44359432_44359438del , CM000667.1:g.44359432_44359438del GRCh37
NC_000005.8:g.44395189_44395195del NCBI36
NG_011446.1:g.34347_34353del

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+29022_325+29028del MANE Select ENSP00000264664.4:n.325+29022_325+29028de...
ENST00000264664.4:c.325+29022_325+29028del ENSP00000264664.4:n.325+29022_325+29028de...
NM_004465.1:c.325+29022_325+29028del NP_004456.1:n.325+29022_325+29028del
XM_005248264.2:c.325+29022_325+29028del XP_005248321.1:n.325+29022_325+29028del
XM_005248264.4:c.325+29022_325+29028del XP_005248321.1:n.325+29022_325+29028del
NM_004465.2:c.325+29022_325+29028del MANE Select NP_004456.1:n.325+29022_325+29028del