Canonical Allele Identifier: CA1075634173
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs3060085

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365360_44365366dup , CM000667.2:g.44365360_44365366dup GRCh38
NC_000005.9:g.44365462_44365468dup , CM000667.1:g.44365462_44365468dup GRCh37
NC_000005.8:g.44401219_44401225dup NCBI36
NG_011446.1:g.28326_28332dup

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+23001_325+23007dup MANE Select ENSP00000264664.4:n.325+23001_325+23007du...
ENST00000264664.4:c.325+23001_325+23007dup ENSP00000264664.4:n.325+23001_325+23007du...
NM_004465.1:c.325+23001_325+23007dup NP_004456.1:n.325+23001_325+23007dup
XM_005248264.2:c.325+23001_325+23007dup XP_005248321.1:n.325+23001_325+23007dup
XM_005248264.4:c.325+23001_325+23007dup XP_005248321.1:n.325+23001_325+23007dup
NM_004465.2:c.325+23001_325+23007dup MANE Select NP_004456.1:n.325+23001_325+23007dup