Canonical Allele Identifier: CA444230967

Gene: FGF10

Linked Data

• gnomAD v4: 5-44305172-A-G
• MyVariant Identifiers: chr5:g.44305274A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305172A>G , CM000667.2:g.44305172A>G	GRCh38
NC_000005.9:g.44305274A>G , CM000667.1:g.44305274A>G	GRCh37
NC_000005.8:g.44341031A>G	NCBI36
NG_011446.1:g.88511T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.450T>C MANE Select	ENSP00000264664.4:p.Cys150=
ENST00000264664.4:c.450T>C	ENSP00000264664.4:p.Cys150=
NM_004465.1:c.450T>C	NP_004456.1:p.Cys150=
XM_005248264.2:c.450T>C	XP_005248321.1:p.Cys150=
XM_005248264.4:c.450T>C	XP_005248321.1:p.Cys150=
NM_004465.2:c.450T>C MANE Select	NP_004456.1:p.Cys150=