Canonical Allele Identifier: CA1075628374
Gene: FGF10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305425_44305432del , CM000667.2:g.44305425_44305432del GRCh38
NC_000005.9:g.44305527_44305534del , CM000667.1:g.44305527_44305534del GRCh37
NC_000005.8:g.44341284_44341291del NCBI36
NG_011446.1:g.88251_88258del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-240_430-233del MANE Select ENSP00000264664.4:n.430-240_430-233del
ENST00000264664.4:c.430-240_430-233del ENSP00000264664.4:n.430-240_430-233del
NM_004465.1:c.430-240_430-233del NP_004456.1:n.430-240_430-233del
XM_005248264.2:c.430-240_430-233del XP_005248321.1:n.430-240_430-233del
XM_005248264.4:c.430-240_430-233del XP_005248321.1:n.430-240_430-233del
NM_004465.2:c.430-240_430-233del MANE Select NP_004456.1:n.430-240_430-233del