Canonical Allele Identifier: CA359697889

Gene: FGF10

Linked Data

• MyVariant Identifiers: chr5:g.44305279C>T (hg19) ; chr5:g.44305177C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305177C>T , CM000667.2:g.44305177C>T	GRCh38
NC_000005.9:g.44305279C>T , CM000667.1:g.44305279C>T	GRCh37
NC_000005.8:g.44341036C>T	NCBI36
NG_011446.1:g.88506G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.445G>A MANE Select	ENSP00000264664.4:p.Asp149Asn
ENST00000264664.4:c.445G>A	ENSP00000264664.4:p.Asp149Asn
NM_004465.1:c.445G>A	NP_004456.1:p.Asp149Asn
XM_005248264.2:c.445G>A	XP_005248321.1:p.Asp149Asn
XM_005248264.4:c.445G>A	XP_005248321.1:p.Asp149Asn
NM_004465.2:c.445G>A MANE Select	NP_004456.1:p.Asp149Asn