Canonical Allele Identifier: CA1543088011
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44335801_44335815delinsTGCTACTTTACCTAG , CM000667.2:g.44335801_44335815delinsTGCTACTTTACCTAG GRCh38
NC_000005.9:g.44335903_44335917delinsTGCTACTTTACCTAG , CM000667.1:g.44335903_44335917delinsTGCTACTTTACCTAG GRCh37
NC_000005.8:g.44371660_44371674delinsTGCTACTTTACCTAG NCBI36
NG_011446.1:g.57868_57882delinsCTAGGTAAAGTAGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.326-25285_326-25271delinsCTAGGTAAAGTAGCA MANE Select ENSP00000264664.4:n.326-25285_326-25271delinsCTAGGTAAAGTAGCA
ENST00000264664.4:c.326-25285_326-25271delinsCTAGGTAAAGTAGCA ENSP00000264664.4:n.326-25285_326-25271delinsCTAGGTAAAGTAGCA
NM_004465.1:c.326-25285_326-25271delinsCTAGGTAAAGTAGCA NP_004456.1:n.326-25285_326-25271delinsCTAGGTAAAGTAGCA
XM_005248264.2:c.326-25285_326-25271delinsCTAGGTAAAGTAGCA XP_005248321.1:n.326-25285_326-25271delinsCTAGGTAAAGTAGCA
XM_005248264.4:c.326-25285_326-25271delinsCTAGGTAAAGTAGCA XP_005248321.1:n.326-25285_326-25271delinsCTAGGTAAAGTAGCA
NM_004465.2:c.326-25285_326-25271delinsCTAGGTAAAGTAGCA MANE Select NP_004456.1:n.326-25285_326-25271delinsCTAGGTAAAGTAGCA