Canonical Allele Identifier: CA2596392343
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs2111867318

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365349_44365350dup , CM000667.2:g.44365349_44365350dup GRCh38
NC_000005.9:g.44365451_44365452dup , CM000667.1:g.44365451_44365452dup GRCh37
NC_000005.8:g.44401208_44401209dup NCBI36
NG_011446.1:g.28333_28334dup

Transcript Alleles

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