Canonical Allele Identifier: CA2578304729
Gene: FGF10 HGNC NCBI

Linked Data

gnomAD v4: 5-44388373-CCTT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388377_44388379del , CM000667.2:g.44388377_44388379del GRCh38
NC_000005.9:g.44388479_44388481del , CM000667.1:g.44388479_44388481del GRCh37
NC_000005.8:g.44424236_44424238del NCBI36
NG_011446.1:g.5307_5309del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.307_309del MANE Select ENSP00000264664.4:p.Lys103del
ENST00000264664.4:c.307_309del ENSP00000264664.4:p.Lys103del
NM_004465.1:c.307_309del NP_004456.1:p.Lys103del
XM_005248264.2:c.307_309del XP_005248321.1:p.Lys103del
XM_005248264.4:c.307_309del XP_005248321.1:p.Lys103del
NM_004465.2:c.307_309del MANE Select NP_004456.1:p.Lys103del
Search 100 bp 5'
Search 100 bp 3'