Canonical Allele Identifier: CA1543136974
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1741823825

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44375094dup , CM000667.2:g.44375094dup GRCh38
NC_000005.9:g.44375196dup , CM000667.1:g.44375196dup GRCh37
NC_000005.8:g.44410953dup NCBI36
NG_011446.1:g.18589dup

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+13264dup MANE Select ENSP00000264664.4:n.325+13264dup
ENST00000264664.4:c.325+13264dup ENSP00000264664.4:n.325+13264dup
NM_004465.1:c.325+13264dup NP_004456.1:n.325+13264dup
XM_005248264.2:c.325+13264dup XP_005248321.1:n.325+13264dup
XM_005248264.4:c.325+13264dup XP_005248321.1:n.325+13264dup
NM_004465.2:c.325+13264dup MANE Select NP_004456.1:n.325+13264dup