Canonical Allele Identifier: CA1543079693

Gene: FGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305157C= , CM000667.2:g.44305157C=	GRCh38
NC_000005.9:g.44305259C= , CM000667.1:g.44305259C=	GRCh37
NC_000005.8:g.44341016C=	NCBI36
NG_011446.1:g.88526G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.465G= MANE Select	ENSP00000264664.4:p.Arg155=
ENST00000264664.4:c.465G=	ENSP00000264664.4:p.Arg155=
NM_004465.1:c.465G=	NP_004456.1:p.Arg155=
XM_005248264.2:c.465G=	XP_005248321.1:p.Arg155=
XM_005248264.4:c.465G=	XP_005248321.1:p.Arg155=
NM_004465.2:c.465G= MANE Select	NP_004456.1:p.Arg155=