Canonical Allele Identifier: CA649973569

Gene: FGF10

Linked Data

• COSMIC: COSN18745937

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44388295_44388296insC , CM000667.2:g.44388295_44388296insC	GRCh38
NC_000005.9:g.44388397_44388398insC , CM000667.1:g.44388397_44388398insC	GRCh37
NC_000005.8:g.44424154_44424155insC	NCBI36
NG_011446.1:g.5387_5388insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.325+62_325+63insG MANE Select	ENSP00000264664.4:n.325+62_325+63insG
ENST00000264664.4:c.325+62_325+63insG	ENSP00000264664.4:n.325+62_325+63insG
NM_004465.1:c.325+62_325+63insG	NP_004456.1:n.325+62_325+63insG
XM_005248264.2:c.325+62_325+63insG	XP_005248321.1:n.325+62_325+63insG
XM_005248264.4:c.325+62_325+63insG	XP_005248321.1:n.325+62_325+63insG
NM_004465.2:c.325+62_325+63insG MANE Select	NP_004456.1:n.325+62_325+63insG