Canonical Allele Identifier: CA1075634132
Gene: FGF10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365350del , CM000667.2:g.44365350del GRCh38
NC_000005.9:g.44365452del , CM000667.1:g.44365452del GRCh37
NC_000005.8:g.44401209del NCBI36
NG_011446.1:g.28333del

Transcript Alleles

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