Canonical Allele Identifier: CA2766095633
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388274G>A , CM000667.2:g.44388274G>A GRCh38
NC_000005.9:g.44388376G>A , CM000667.1:g.44388376G>A GRCh37
NC_000005.8:g.44424133G>A NCBI36
NG_011446.1:g.5409C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.325+84C>T MANE Select ENSP00000264664.4:n.325+84C>T
ENST00000264664.4:c.325+84C>T ENSP00000264664.4:n.325+84C>T
NM_004465.1:c.325+84C>T NP_004456.1:n.325+84C>T
XM_005248264.2:c.325+84C>T XP_005248321.1:n.325+84C>T
XM_005248264.4:c.325+84C>T XP_005248321.1:n.325+84C>T
NM_004465.2:c.325+84C>T MANE Select NP_004456.1:n.325+84C>T