Canonical Allele Identifier: CA2673772772

Gene: FGF10

Linked Data

• gnomAD v4: 5-44305282-ATTCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305283_44305286del , CM000667.2:g.44305283_44305286del	GRCh38
NC_000005.9:g.44305385_44305388del , CM000667.1:g.44305385_44305388del	GRCh37
NC_000005.8:g.44341142_44341145del	NCBI36
NG_011446.1:g.88397_88400del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.430-94_430-91del MANE Select	ENSP00000264664.4:n.430-94_430-91del
ENST00000264664.4:c.430-94_430-91del	ENSP00000264664.4:n.430-94_430-91del
NM_004465.1:c.430-94_430-91del	NP_004456.1:n.430-94_430-91del
XM_005248264.2:c.430-94_430-91del	XP_005248321.1:n.430-94_430-91del
XM_005248264.4:c.430-94_430-91del	XP_005248321.1:n.430-94_430-91del
NM_004465.2:c.430-94_430-91del MANE Select	NP_004456.1:n.430-94_430-91del