Canonical Allele Identifier: CA1543136969

Gene: FGF10

Linked Data

• dbSNP Id: rs1741823775

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44375090_44375098del , CM000667.2:g.44375090_44375098del	GRCh38
NC_000005.9:g.44375192_44375200del , CM000667.1:g.44375192_44375200del	GRCh37
NC_000005.8:g.44410949_44410957del	NCBI36
NG_011446.1:g.18585_18593del

Transcript Alleles

HGVS	Amino-acid change
ENST00000264664.5:c.325+13260_325+13268del MANE Select	ENSP00000264664.4:n.325+13260_325+13268del
ENST00000264664.4:c.325+13260_325+13268del	ENSP00000264664.4:n.325+13260_325+13268del
NM_004465.1:c.325+13260_325+13268del	NP_004456.1:n.325+13260_325+13268del
XM_005248264.2:c.325+13260_325+13268del	XP_005248321.1:n.325+13260_325+13268del
XM_005248264.4:c.325+13260_325+13268del	XP_005248321.1:n.325+13260_325+13268del
NM_004465.2:c.325+13260_325+13268del MANE Select	NP_004456.1:n.325+13260_325+13268del