Canonical Allele Identifier: CA444230980
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1579935089

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365349_44365350insAA , CM000667.2:g.44365349_44365350insAA GRCh38
NC_000005.9:g.44365451_44365452insAA , CM000667.1:g.44365451_44365452insAA GRCh37
NC_000005.8:g.44401208_44401209insAA NCBI36
NG_011446.1:g.28333_28334insTT

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+23008_325+23009insTT MANE Select ENSP00000264664.4:n.325+23008_325+23009in...
ENST00000264664.4:c.325+23008_325+23009insTT ENSP00000264664.4:n.325+23008_325+23009in...
NM_004465.1:c.325+23008_325+23009insTT NP_004456.1:n.325+23008_325+23009insTT
XM_005248264.2:c.325+23008_325+23009insTT XP_005248321.1:n.325+23008_325+23009insTT...
XM_005248264.4:c.325+23008_325+23009insTT XP_005248321.1:n.325+23008_325+23009insTT...
NM_004465.2:c.325+23008_325+23009insTT MANE Select NP_004456.1:n.325+23008_325+23009insTT