Canonical Allele Identifier: CA359697902

Gene: FGF10

Linked Data

• MyVariant Identifiers: chr5:g.44305284T>G (hg19) ; chr5:g.44305182T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305182T>G , CM000667.2:g.44305182T>G	GRCh38
NC_000005.9:g.44305284T>G , CM000667.1:g.44305284T>G	GRCh37
NC_000005.8:g.44341041T>G	NCBI36
NG_011446.1:g.88501A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.440A>C MANE Select	ENSP00000264664.4:p.Asn147Thr
ENST00000264664.4:c.440A>C	ENSP00000264664.4:p.Asn147Thr
NM_004465.1:c.440A>C	NP_004456.1:p.Asn147Thr
XM_005248264.2:c.440A>C	XP_005248321.1:p.Asn147Thr
XM_005248264.4:c.440A>C	XP_005248321.1:p.Asn147Thr
NM_004465.2:c.440A>C MANE Select	NP_004456.1:p.Asn147Thr