Canonical Allele Identifier: CA2708905153
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs2111867354

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365350_44365351insCA , CM000667.2:g.44365350_44365351insCA GRCh38
NC_000005.9:g.44365452_44365453insCA , CM000667.1:g.44365452_44365453insCA GRCh37
NC_000005.8:g.44401209_44401210insCA NCBI36
NG_011446.1:g.28332_28333insTG

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+23007_325+23008insTG MANE Select ENSP00000264664.4:n.325+23007_325+23008in...
ENST00000264664.4:c.325+23007_325+23008insTG ENSP00000264664.4:n.325+23007_325+23008in...
NM_004465.1:c.325+23007_325+23008insTG NP_004456.1:n.325+23007_325+23008insTG
XM_005248264.2:c.325+23007_325+23008insTG XP_005248321.1:n.325+23007_325+23008insTG...
XM_005248264.4:c.325+23007_325+23008insTG XP_005248321.1:n.325+23007_325+23008insTG...
NM_004465.2:c.325+23007_325+23008insTG MANE Select NP_004456.1:n.325+23007_325+23008insTG