Canonical Allele Identifier: CA811000288

Gene: FGF10

Linked Data

• dbSNP Id: rs1299422712
• MyVariant Identifiers: chr5:g.44365462_44365463insAG (hg19) ; chr5:g.44365360_44365361insAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44365361_44365362insGA , CM000667.2:g.44365361_44365362insGA	GRCh38
NC_000005.9:g.44365463_44365464insGA , CM000667.1:g.44365463_44365464insGA	GRCh37
NC_000005.8:g.44401220_44401221insGA	NCBI36
NG_011446.1:g.28322_28323insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.325+22997_325+22998insCT MANE Select	ENSP00000264664.4:n.325+22997_325+22998insCT
ENST00000264664.4:c.325+22997_325+22998insCT	ENSP00000264664.4:n.325+22997_325+22998insCT
NM_004465.1:c.325+22997_325+22998insCT	NP_004456.1:n.325+22997_325+22998insCT
XM_005248264.2:c.325+22997_325+22998insCT	XP_005248321.1:n.325+22997_325+22998insCT
XM_005248264.4:c.325+22997_325+22998insCT	XP_005248321.1:n.325+22997_325+22998insCT
NM_004465.2:c.325+22997_325+22998insCT MANE Select	NP_004456.1:n.325+22997_325+22998insCT