Canonical Allele Identifier: CA915124544

Gene: FGF10

Linked Data

• dbSNP Id: rs1561205646
• gnomAD v2: 5-44335903-TGCTACTTTACCTAG-T
• gnomAD v3: 5-44335801-TGCTACTTTACCTAG-T
• gnomAD v4: 5-44335801-TGCTACTTTACCTAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44335804_44335817del , CM000667.2:g.44335804_44335817del	GRCh38
NC_000005.9:g.44335906_44335919del , CM000667.1:g.44335906_44335919del	GRCh37
NC_000005.8:g.44371663_44371676del	NCBI36
NG_011446.1:g.57868_57881del

Transcript Alleles

HGVS	Amino-acid change
ENST00000264664.5:c.326-25285_326-25272del MANE Select	ENSP00000264664.4:n.326-25285_326-25272del
ENST00000264664.4:c.326-25285_326-25272del	ENSP00000264664.4:n.326-25285_326-25272del
NM_004465.1:c.326-25285_326-25272del	NP_004456.1:n.326-25285_326-25272del
XM_005248264.2:c.326-25285_326-25272del	XP_005248321.1:n.326-25285_326-25272del
XM_005248264.4:c.326-25285_326-25272del	XP_005248321.1:n.326-25285_326-25272del
NM_004465.2:c.326-25285_326-25272del MANE Select	NP_004456.1:n.326-25285_326-25272del