Canonical Allele Identifier: CA444400486

Gene: FGF10

Linked Data

• MyVariant Identifiers: chr5:g.44388560T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44388458T>C , CM000667.2:g.44388458T>C	GRCh38
NC_000005.9:g.44388560T>C , CM000667.1:g.44388560T>C	GRCh37
NC_000005.8:g.44424317T>C	NCBI36
NG_011446.1:g.5225A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264664.5:c.225A>G MANE Select	ENSP00000264664.4:p.Gly75=
ENST00000264664.4:c.225A>G	ENSP00000264664.4:p.Gly75=
NM_004465.1:c.225A>G	NP_004456.1:p.Gly75=
XM_005248264.2:c.225A>G	XP_005248321.1:p.Gly75=
XM_005248264.4:c.225A>G	XP_005248321.1:p.Gly75=
NM_004465.2:c.225A>G MANE Select	NP_004456.1:p.Gly75=