Canonical Allele Identifier: CA810994803

Gene: FGF10

Linked Data

• dbSNP Id: rs1440653288
• gnomAD v3: 5-44305536-AAAG-A
• gnomAD v4: 5-44305536-AAAG-A
• MyVariant Identifiers: chr5:g.44305639_44305641del (hg19) ; chr5:g.44305537_44305539del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305539_44305541del , CM000667.2:g.44305539_44305541del	GRCh38
NC_000005.9:g.44305641_44305643del , CM000667.1:g.44305641_44305643del	GRCh37
NC_000005.8:g.44341398_44341400del	NCBI36
NG_011446.1:g.88144_88146del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.430-347_430-345del MANE Select	ENSP00000264664.4:n.430-347_430-345del
ENST00000264664.4:c.430-347_430-345del	ENSP00000264664.4:n.430-347_430-345del
NM_004465.1:c.430-347_430-345del	NP_004456.1:n.430-347_430-345del
XM_005248264.2:c.430-347_430-345del	XP_005248321.1:n.430-347_430-345del
XM_005248264.4:c.430-347_430-345del	XP_005248321.1:n.430-347_430-345del
NM_004465.2:c.430-347_430-345del MANE Select	NP_004456.1:n.430-347_430-345del