Canonical Allele Identifier: CA2527478735
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365349_44365350insTAAA , CM000667.2:g.44365349_44365350insTAAA GRCh38
NC_000005.9:g.44365451_44365452insTAAA , CM000667.1:g.44365451_44365452insTAAA GRCh37
NC_000005.8:g.44401208_44401209insTAAA NCBI36
NG_011446.1:g.28333_28334insTTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+23008_325+23009insTTTA MANE Select ENSP00000264664.4:n.325+23008_325+23009in...
ENST00000264664.4:c.325+23008_325+23009insTTTA ENSP00000264664.4:n.325+23008_325+23009in...
NM_004465.1:c.325+23008_325+23009insTTTA NP_004456.1:n.325+23008_325+23009insTTTA
XM_005248264.2:c.325+23008_325+23009insTTTA XP_005248321.1:n.325+23008_325+23009insTT...
XM_005248264.4:c.325+23008_325+23009insTTTA XP_005248321.1:n.325+23008_325+23009insTT...
NM_004465.2:c.325+23008_325+23009insTTTA MANE Select NP_004456.1:n.325+23008_325+23009insTTTA