Canonical Allele Identifier: CA359697838

Gene: FGF10

Linked Data

• MyVariant Identifiers: chr5:g.44305259C>A (hg19) ; chr5:g.44305157C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305157C>A , CM000667.2:g.44305157C>A	GRCh38
NC_000005.9:g.44305259C>A , CM000667.1:g.44305259C>A	GRCh37
NC_000005.8:g.44341016C>A	NCBI36
NG_011446.1:g.88526G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.465G>T MANE Select	ENSP00000264664.4:p.Arg155Ser
ENST00000264664.4:c.465G>T	ENSP00000264664.4:p.Arg155Ser
NM_004465.1:c.465G>T	NP_004456.1:p.Arg155Ser
XM_005248264.2:c.465G>T	XP_005248321.1:p.Arg155Ser
XM_005248264.4:c.465G>T	XP_005248321.1:p.Arg155Ser
NM_004465.2:c.465G>T MANE Select	NP_004456.1:p.Arg155Ser