Canonical Allele Identifier: CA359697896

Gene: FGF10

Linked Data

• gnomAD v4: 5-44305180-T-A
• MyVariant Identifiers: chr5:g.44305282T>A (hg19) ; chr5:g.44305180T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.442A>T MANE Select	ENSP00000264664.4:p.Asn148Tyr
ENST00000264664.4:c.442A>T	ENSP00000264664.4:p.Asn148Tyr
NM_004465.1:c.442A>T	NP_004456.1:p.Asn148Tyr
XM_005248264.2:c.442A>T	XP_005248321.1:p.Asn148Tyr
XM_005248264.4:c.442A>T	XP_005248321.1:p.Asn148Tyr
NM_004465.2:c.442A>T MANE Select	NP_004456.1:p.Asn148Tyr