Canonical Allele Identifier: CA1543080149

Gene: FGF10

Linked Data

• dbSNP Id: rs1740054844

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44305485_44305488del , CM000667.2:g.44305485_44305488del	GRCh38
NC_000005.9:g.44305587_44305590del , CM000667.1:g.44305587_44305590del	GRCh37
NC_000005.8:g.44341344_44341347del	NCBI36
NG_011446.1:g.88197_88200del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264664.5:c.430-294_430-291del MANE Select	ENSP00000264664.4:n.430-294_430-291del
ENST00000264664.4:c.430-294_430-291del	ENSP00000264664.4:n.430-294_430-291del
NM_004465.1:c.430-294_430-291del	NP_004456.1:n.430-294_430-291del
XM_005248264.2:c.430-294_430-291del	XP_005248321.1:n.430-294_430-291del
XM_005248264.4:c.430-294_430-291del	XP_005248321.1:n.430-294_430-291del
NM_004465.2:c.430-294_430-291del MANE Select	NP_004456.1:n.430-294_430-291del