Canonical Allele Identifier: CA1543080498

Gene: FGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305724_44305725delinsAG , CM000667.2:g.44305724_44305725delinsAG	GRCh38
NC_000005.9:g.44305826_44305827delinsAG , CM000667.1:g.44305826_44305827delinsAG	GRCh37
NC_000005.8:g.44341583_44341584delinsAG	NCBI36
NG_011446.1:g.87958_87959delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.430-533_430-532delinsCT MANE Select	ENSP00000264664.4:n.430-533_430-532delinsCT
ENST00000264664.4:c.430-533_430-532delinsCT	ENSP00000264664.4:n.430-533_430-532delinsCT
NM_004465.1:c.430-533_430-532delinsCT	NP_004456.1:n.430-533_430-532delinsCT
XM_005248264.2:c.430-533_430-532delinsCT	XP_005248321.1:n.430-533_430-532delinsCT
XM_005248264.4:c.430-533_430-532delinsCT	XP_005248321.1:n.430-533_430-532delinsCT
NM_004465.2:c.430-533_430-532delinsCT MANE Select	NP_004456.1:n.430-533_430-532delinsCT