Canonical Allele Identifier: CA1543090411

Gene: FGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44388296_44388297delinsTC , CM000667.2:g.44388296_44388297delinsTC	GRCh38
NC_000005.9:g.44388398_44388399delinsTC , CM000667.1:g.44388398_44388399delinsTC	GRCh37
NC_000005.8:g.44424155_44424156delinsTC	NCBI36
NG_011446.1:g.5386_5387delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.325+61_325+62delinsGA MANE Select	ENSP00000264664.4:n.325+61_325+62delinsGA
ENST00000264664.4:c.325+61_325+62delinsGA	ENSP00000264664.4:n.325+61_325+62delinsGA
NM_004465.1:c.325+61_325+62delinsGA	NP_004456.1:n.325+61_325+62delinsGA
XM_005248264.2:c.325+61_325+62delinsGA	XP_005248321.1:n.325+61_325+62delinsGA
XM_005248264.4:c.325+61_325+62delinsGA	XP_005248321.1:n.325+61_325+62delinsGA
NM_004465.2:c.325+61_325+62delinsGA MANE Select	NP_004456.1:n.325+61_325+62delinsGA