Canonical Allele Identifier: CA1543124853

Gene: FGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44359554_44359558delinsGGGCT , CM000667.2:g.44359554_44359558delinsGGGCT	GRCh38
NC_000005.9:g.44359656_44359660delinsGGGCT , CM000667.1:g.44359656_44359660delinsGGGCT	GRCh37
NC_000005.8:g.44395413_44395417delinsGGGCT	NCBI36
NG_011446.1:g.34125_34129delinsAGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.325+28800_325+28804delinsAGCCC MANE Select	ENSP00000264664.4:n.325+28800_325+28804delinsAGCCC
ENST00000264664.4:c.325+28800_325+28804delinsAGCCC	ENSP00000264664.4:n.325+28800_325+28804delinsAGCCC
NM_004465.1:c.325+28800_325+28804delinsAGCCC	NP_004456.1:n.325+28800_325+28804delinsAGCCC
XM_005248264.2:c.325+28800_325+28804delinsAGCCC	XP_005248321.1:n.325+28800_325+28804delinsAGCCC
XM_005248264.4:c.325+28800_325+28804delinsAGCCC	XP_005248321.1:n.325+28800_325+28804delinsAGCCC
NM_004465.2:c.325+28800_325+28804delinsAGCCC MANE Select	NP_004456.1:n.325+28800_325+28804delinsAGCCC