Canonical Allele Identifier: CA1075634118
Gene: FGF10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365347_44365350del , CM000667.2:g.44365347_44365350del GRCh38
NC_000005.9:g.44365449_44365452del , CM000667.1:g.44365449_44365452del GRCh37
NC_000005.8:g.44401206_44401209del NCBI36
NG_011446.1:g.28333_28336del

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+23008_325+23011del MANE Select ENSP00000264664.4:n.325+23008_325+23011de...
ENST00000264664.4:c.325+23008_325+23011del ENSP00000264664.4:n.325+23008_325+23011de...
NM_004465.1:c.325+23008_325+23011del NP_004456.1:n.325+23008_325+23011del
XM_005248264.2:c.325+23008_325+23011del XP_005248321.1:n.325+23008_325+23011del
XM_005248264.4:c.325+23008_325+23011del XP_005248321.1:n.325+23008_325+23011del
NM_004465.2:c.325+23008_325+23011del MANE Select NP_004456.1:n.325+23008_325+23011del