Canonical Allele Identifier: CA559293710

Gene: FGF10

Linked Data

• dbSNP Id: rs1179074723
• gnomAD v2: 5-44305411-T-TAAG
• gnomAD v3: 5-44305309-T-TAAG
• gnomAD v4: 5-44305309-T-TAAG
• MyVariant Identifiers: chr5:g.44305411_44305412insAAG (hg19) ; chr5:g.44305309_44305310insAAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305310_44305312dup , CM000667.2:g.44305310_44305312dup	GRCh38
NC_000005.9:g.44305412_44305414dup , CM000667.1:g.44305412_44305414dup	GRCh37
NC_000005.8:g.44341169_44341171dup	NCBI36
NG_011446.1:g.88371_88373dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.430-120_430-118dup MANE Select	ENSP00000264664.4:n.430-120_430-118dup
ENST00000264664.4:c.430-120_430-118dup	ENSP00000264664.4:n.430-120_430-118dup
NM_004465.1:c.430-120_430-118dup	NP_004456.1:n.430-120_430-118dup
XM_005248264.2:c.430-120_430-118dup	XP_005248321.1:n.430-120_430-118dup
XM_005248264.4:c.430-120_430-118dup	XP_005248321.1:n.430-120_430-118dup
NM_004465.2:c.430-120_430-118dup MANE Select	NP_004456.1:n.430-120_430-118dup