Canonical Allele Identifier: CA1543079712

Gene: FGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305170T= , CM000667.2:g.44305170T=	GRCh38
NC_000005.9:g.44305272T= , CM000667.1:g.44305272T=	GRCh37
NC_000005.8:g.44341029T=	NCBI36
NG_011446.1:g.88513A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.452A= MANE Select	ENSP00000264664.4:p.Lys151=
ENST00000264664.4:c.452A=	ENSP00000264664.4:p.Lys151=
NM_004465.1:c.452A=	NP_004456.1:p.Lys151=
XM_005248264.2:c.452A=	XP_005248321.1:p.Lys151=
XM_005248264.4:c.452A=	XP_005248321.1:p.Lys151=
NM_004465.2:c.452A= MANE Select	NP_004456.1:p.Lys151=