Canonical Allele Identifier: CA1543080050
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305394_44305399delinsACATTT , CM000667.2:g.44305394_44305399delinsACATTT GRCh38
NC_000005.9:g.44305496_44305501delinsACATTT , CM000667.1:g.44305496_44305501delinsACATTT GRCh37
NC_000005.8:g.44341253_44341258delinsACATTT NCBI36
NG_011446.1:g.88284_88289delinsAAATGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-207_430-202delinsAAATGT MANE Select ENSP00000264664.4:n.430-207_430-202delinsAAATGT
ENST00000264664.4:c.430-207_430-202delinsAAATGT ENSP00000264664.4:n.430-207_430-202delinsAAATGT
NM_004465.1:c.430-207_430-202delinsAAATGT NP_004456.1:n.430-207_430-202delinsAAATGT
XM_005248264.2:c.430-207_430-202delinsAAATGT XP_005248321.1:n.430-207_430-202delinsAAATGT
XM_005248264.4:c.430-207_430-202delinsAAATGT XP_005248321.1:n.430-207_430-202delinsAAATGT
NM_004465.2:c.430-207_430-202delinsAAATGT MANE Select NP_004456.1:n.430-207_430-202delinsAAATGT