Canonical Allele Identifier: CA359697907

Gene: FGF10

Linked Data

• MyVariant Identifiers: chr5:g.44305286A>T (hg19) ; chr5:g.44305184A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305184A>T , CM000667.2:g.44305184A>T	GRCh38
NC_000005.9:g.44305286A>T , CM000667.1:g.44305286A>T	GRCh37
NC_000005.8:g.44341043A>T	NCBI36
NG_011446.1:g.88499T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.438T>A MANE Select	ENSP00000264664.4:p.Phe146Leu
ENST00000264664.4:c.438T>A	ENSP00000264664.4:p.Phe146Leu
NM_004465.1:c.438T>A	NP_004456.1:p.Phe146Leu
XM_005248264.2:c.438T>A	XP_005248321.1:p.Phe146Leu
XM_005248264.4:c.438T>A	XP_005248321.1:p.Phe146Leu
NM_004465.2:c.438T>A MANE Select	NP_004456.1:p.Phe146Leu