Canonical Allele Identifier: CA1543090390

Gene: FGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44388294T= , CM000667.2:g.44388294T=	GRCh38
NC_000005.9:g.44388396T= , CM000667.1:g.44388396T=	GRCh37
NC_000005.8:g.44424153T=	NCBI36
NG_011446.1:g.5389A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.325+64A= MANE Select	ENSP00000264664.4:n.325+64A=
ENST00000264664.4:c.325+64A=	ENSP00000264664.4:n.325+64A=
NM_004465.1:c.325+64A=	NP_004456.1:n.325+64A=
XM_005248264.2:c.325+64A=	XP_005248321.1:n.325+64A=
XM_005248264.4:c.325+64A=	XP_005248321.1:n.325+64A=
NM_004465.2:c.325+64A= MANE Select	NP_004456.1:n.325+64A=