Canonical Allele Identifier: CA359697882

Gene: FGF10

Linked Data

• MyVariant Identifiers: chr5:g.44305277G>C (hg19) ; chr5:g.44305175G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305175G>C , CM000667.2:g.44305175G>C	GRCh38
NC_000005.9:g.44305277G>C , CM000667.1:g.44305277G>C	GRCh37
NC_000005.8:g.44341034G>C	NCBI36
NG_011446.1:g.88508C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.447C>G MANE Select	ENSP00000264664.4:p.Asp149Glu
ENST00000264664.4:c.447C>G	ENSP00000264664.4:p.Asp149Glu
NM_004465.1:c.447C>G	NP_004456.1:p.Asp149Glu
XM_005248264.2:c.447C>G	XP_005248321.1:p.Asp149Glu
XM_005248264.4:c.447C>G	XP_005248321.1:p.Asp149Glu
NM_004465.2:c.447C>G MANE Select	NP_004456.1:p.Asp149Glu