Canonical Allele Identifier: CA1543080598
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305748_44305749delinsTA , CM000667.2:g.44305748_44305749delinsTA GRCh38
NC_000005.9:g.44305850_44305851delinsTA , CM000667.1:g.44305850_44305851delinsTA GRCh37
NC_000005.8:g.44341607_44341608delinsTA NCBI36
NG_011446.1:g.87934_87935delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-557_430-556delinsTA MANE Select ENSP00000264664.4:n.430-557_430-556delinsTA
ENST00000264664.4:c.430-557_430-556delinsTA ENSP00000264664.4:n.430-557_430-556delinsTA
NM_004465.1:c.430-557_430-556delinsTA NP_004456.1:n.430-557_430-556delinsTA
XM_005248264.2:c.430-557_430-556delinsTA XP_005248321.1:n.430-557_430-556delinsTA
XM_005248264.4:c.430-557_430-556delinsTA XP_005248321.1:n.430-557_430-556delinsTA
NM_004465.2:c.430-557_430-556delinsTA MANE Select NP_004456.1:n.430-557_430-556delinsTA