Canonical Allele Identifier: CA2673772734
Gene: FGF10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305207_44305208del , CM000667.2:g.44305207_44305208del GRCh38
NC_000005.9:g.44305309_44305310del , CM000667.1:g.44305309_44305310del GRCh37
NC_000005.8:g.44341066_44341067del NCBI36
NG_011446.1:g.88476_88477del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-15_430-14del MANE Select ENSP00000264664.4:n.430-15_430-14del
ENST00000264664.4:c.430-15_430-14del ENSP00000264664.4:n.430-15_430-14del
NM_004465.1:c.430-15_430-14del NP_004456.1:n.430-15_430-14del
XM_005248264.2:c.430-15_430-14del XP_005248321.1:n.430-15_430-14del
XM_005248264.4:c.430-15_430-14del XP_005248321.1:n.430-15_430-14del
NM_004465.2:c.430-15_430-14del MANE Select NP_004456.1:n.430-15_430-14del