Canonical Allele Identifier: CA1543090574
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388359G= , CM000667.2:g.44388359G= GRCh38
NC_000005.9:g.44388461G= , CM000667.1:g.44388461G= GRCh37
NC_000005.8:g.44424218G= NCBI36
NG_011446.1:g.5324C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.324C= MANE Select ENSP00000264664.4:p.Tyr108=
ENST00000264664.4:c.324C= ENSP00000264664.4:p.Tyr108=
NM_004465.1:c.324C= NP_004456.1:p.Tyr108=
XM_005248264.2:c.324C= XP_005248321.1:p.Tyr108=
XM_005248264.4:c.324C= XP_005248321.1:p.Tyr108=
NM_004465.2:c.324C= MANE Select NP_004456.1:p.Tyr108=