Canonical Allele Identifier: CA2708903600

Gene: FGF10

Linked Data

• dbSNP Id: rs2111848890

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44359553_44359554del , CM000667.2:g.44359553_44359554del	GRCh38
NC_000005.9:g.44359655_44359656del , CM000667.1:g.44359655_44359656del	GRCh37
NC_000005.8:g.44395412_44395413del	NCBI36
NG_011446.1:g.34129_34130del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.325+28804_325+28805del MANE Select	ENSP00000264664.4:n.325+28804_325+28805del
ENST00000264664.4:c.325+28804_325+28805del	ENSP00000264664.4:n.325+28804_325+28805del
NM_004465.1:c.325+28804_325+28805del	NP_004456.1:n.325+28804_325+28805del
XM_005248264.2:c.325+28804_325+28805del	XP_005248321.1:n.325+28804_325+28805del
XM_005248264.4:c.325+28804_325+28805del	XP_005248321.1:n.325+28804_325+28805del
NM_004465.2:c.325+28804_325+28805del MANE Select	NP_004456.1:n.325+28804_325+28805del