Canonical Allele Identifier: CA1543128944

Gene: FGF10

Linked Data

• dbSNP Id: rs1741582621

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44365363_44365364insCA , CM000667.2:g.44365363_44365364insCA	GRCh38
NC_000005.9:g.44365465_44365466insCA , CM000667.1:g.44365465_44365466insCA	GRCh37
NC_000005.8:g.44401222_44401223insCA	NCBI36
NG_011446.1:g.28320_28321insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.325+22995_325+22996insGT MANE Select	ENSP00000264664.4:n.325+22995_325+22996insGT
ENST00000264664.4:c.325+22995_325+22996insGT	ENSP00000264664.4:n.325+22995_325+22996insGT
NM_004465.1:c.325+22995_325+22996insGT	NP_004456.1:n.325+22995_325+22996insGT
XM_005248264.2:c.325+22995_325+22996insGT	XP_005248321.1:n.325+22995_325+22996insGT
XM_005248264.4:c.325+22995_325+22996insGT	XP_005248321.1:n.325+22995_325+22996insGT
NM_004465.2:c.325+22995_325+22996insGT MANE Select	NP_004456.1:n.325+22995_325+22996insGT