Canonical Allele Identifier: CA2578304719
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388275del , CM000667.2:g.44388275del GRCh38
NC_000005.9:g.44388377del , CM000667.1:g.44388377del GRCh37
NC_000005.8:g.44424134del NCBI36
NG_011446.1:g.5409del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.325+84del MANE Select ENSP00000264664.4:n.325+84del
ENST00000264664.4:c.325+84del ENSP00000264664.4:n.325+84del
NM_004465.1:c.325+84del NP_004456.1:n.325+84del
XM_005248264.2:c.325+84del XP_005248321.1:n.325+84del
XM_005248264.4:c.325+84del XP_005248321.1:n.325+84del
NM_004465.2:c.325+84del MANE Select NP_004456.1:n.325+84del