Canonical Allele Identifier: CA1543129014
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365515T= , CM000667.2:g.44365515T= GRCh38
NC_000005.9:g.44365617T= , CM000667.1:g.44365617T= GRCh37
NC_000005.8:g.44401374T= NCBI36
NG_011446.1:g.28168A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.325+22843A= MANE Select ENSP00000264664.4:n.325+22843A=
ENST00000264664.4:c.325+22843A= ENSP00000264664.4:n.325+22843A=
NM_004465.1:c.325+22843A= NP_004456.1:n.325+22843A=
XM_005248264.2:c.325+22843A= XP_005248321.1:n.325+22843A=
XM_005248264.4:c.325+22843A= XP_005248321.1:n.325+22843A=
NM_004465.2:c.325+22843A= MANE Select NP_004456.1:n.325+22843A=