Canonical Allele Identifier: CA3258493

Gene: FGF10

Linked Data

• dbSNP Id: rs753414988
• ExAC: 5:44305310 AGAATCTTTTATT / A
• gnomAD v2: 5-44305310-AGAATCTTTTATT-A
• MyVariant Identifiers: chr5:g.44305311_44305322del (hg19) ; chr5:g.44305209_44305220del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305209_44305220del , CM000667.2:g.44305209_44305220del	GRCh38
NC_000005.9:g.44305311_44305322del , CM000667.1:g.44305311_44305322del	GRCh37
NC_000005.8:g.44341068_44341079del	NCBI36
NG_011446.1:g.88463_88474del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.430-28_430-17del MANE Select	ENSP00000264664.4:n.430-28_430-17del
ENST00000264664.4:c.430-28_430-17del	ENSP00000264664.4:n.430-28_430-17del
NM_004465.1:c.430-28_430-17del	NP_004456.1:n.430-28_430-17del
XM_005248264.2:c.430-28_430-17del	XP_005248321.1:n.430-28_430-17del
XM_005248264.4:c.430-28_430-17del	XP_005248321.1:n.430-28_430-17del
NM_004465.2:c.430-28_430-17del MANE Select	NP_004456.1:n.430-28_430-17del