Canonical Allele Identifier: CA810994869
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1448175701
MyVariant Identifiers: chr5:g.44305762_44305763del (hg19) chr5:g.44305660_44305661del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305669_44305670del , CM000667.2:g.44305669_44305670del GRCh38
NC_000005.9:g.44305771_44305772del , CM000667.1:g.44305771_44305772del GRCh37
NC_000005.8:g.44341528_44341529del NCBI36
NG_011446.1:g.88022_88023del

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.430-469_430-468del MANE Select ENSP00000264664.4:n.430-469_430-468del
ENST00000264664.4:c.430-469_430-468del ENSP00000264664.4:n.430-469_430-468del
NM_004465.1:c.430-469_430-468del NP_004456.1:n.430-469_430-468del
XM_005248264.2:c.430-469_430-468del XP_005248321.1:n.430-469_430-468del
XM_005248264.4:c.430-469_430-468del XP_005248321.1:n.430-469_430-468del
NM_004465.2:c.430-469_430-468del MANE Select NP_004456.1:n.430-469_430-468del
Search 100 bp 5'
Search 100 bp 3'