Canonical Allele Identifier: CA359697895

Gene: FGF10

Linked Data

• MyVariant Identifiers: chr5:g.44305282T>G (hg19) ; chr5:g.44305180T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305180T>G , CM000667.2:g.44305180T>G	GRCh38
NC_000005.9:g.44305282T>G , CM000667.1:g.44305282T>G	GRCh37
NC_000005.8:g.44341039T>G	NCBI36
NG_011446.1:g.88503A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.442A>C MANE Select	ENSP00000264664.4:p.Asn148His
ENST00000264664.4:c.442A>C	ENSP00000264664.4:p.Asn148His
NM_004465.1:c.442A>C	NP_004456.1:p.Asn148His
XM_005248264.2:c.442A>C	XP_005248321.1:p.Asn148His
XM_005248264.4:c.442A>C	XP_005248321.1:p.Asn148His
NM_004465.2:c.442A>C MANE Select	NP_004456.1:p.Asn148His