Canonical Allele Identifier: CA1543079707

Gene: FGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305169C= , CM000667.2:g.44305169C=	GRCh38
NC_000005.9:g.44305271C= , CM000667.1:g.44305271C=	GRCh37
NC_000005.8:g.44341028C=	NCBI36
NG_011446.1:g.88514G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.453G= MANE Select	ENSP00000264664.4:p.Lys151=
ENST00000264664.4:c.453G=	ENSP00000264664.4:p.Lys151=
NM_004465.1:c.453G=	NP_004456.1:p.Lys151=
XM_005248264.2:c.453G=	XP_005248321.1:p.Lys151=
XM_005248264.4:c.453G=	XP_005248321.1:p.Lys151=
NM_004465.2:c.453G= MANE Select	NP_004456.1:p.Lys151=