Canonical Allele Identifier: CA811000283

Gene: FGF10

Linked Data

• dbSNP Id: rs3060085
• gnomAD v3: 5-44365350-CAA-C
• gnomAD v4: 5-44365350-CAA-C
• MyVariant Identifiers: chr5:g.44365453_44365454del (hg19) ; chr5:g.44365351_44365352del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44365365_44365366del , CM000667.2:g.44365365_44365366del	GRCh38
NC_000005.9:g.44365467_44365468del , CM000667.1:g.44365467_44365468del	GRCh37
NC_000005.8:g.44401224_44401225del	NCBI36
NG_011446.1:g.28331_28332del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.325+23006_325+23007del MANE Select	ENSP00000264664.4:n.325+23006_325+23007del
ENST00000264664.4:c.325+23006_325+23007del	ENSP00000264664.4:n.325+23006_325+23007del
NM_004465.1:c.325+23006_325+23007del	NP_004456.1:n.325+23006_325+23007del
XM_005248264.2:c.325+23006_325+23007del	XP_005248321.1:n.325+23006_325+23007del
XM_005248264.4:c.325+23006_325+23007del	XP_005248321.1:n.325+23006_325+23007del
NM_004465.2:c.325+23006_325+23007del MANE Select	NP_004456.1:n.325+23006_325+23007del