Canonical Allele Identifier: CA444230981
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1579935089

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365349_44365350insAAA , CM000667.2:g.44365349_44365350insAAA GRCh38
NC_000005.9:g.44365451_44365452insAAA , CM000667.1:g.44365451_44365452insAAA GRCh37
NC_000005.8:g.44401208_44401209insAAA NCBI36
NG_011446.1:g.28333_28334insTTT

Transcript Alleles

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