Canonical Allele Identifier: CA2766093784
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305257_44305258insAACACCAAACACACCCAACA , CM000667.2:g.44305257_44305258insAACACCAAACACACCCAACA GRCh38
NC_000005.9:g.44305359_44305360insAACACCAAACACACCCAACA , CM000667.1:g.44305359_44305360insAACACCAAACACACCCAACA GRCh37
NC_000005.8:g.44341116_44341117insAACACCAAACACACCCAACA NCBI36
NG_011446.1:g.88425_88426insTGTTGGGTGTGTTTGGTGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.430-66_430-65insTGTTGGGTGTGTTTGGTGTT MANE Select ENSP00000264664.4:n.430-66_430-65insTGTTGGGTGTGTTTGGTGTT
ENST00000264664.4:c.430-66_430-65insTGTTGGGTGTGTTTGGTGTT ENSP00000264664.4:n.430-66_430-65insTGTTGGGTGTGTTTGGTGTT
NM_004465.1:c.430-66_430-65insTGTTGGGTGTGTTTGGTGTT NP_004456.1:n.430-66_430-65insTGTTGGGTGTGTTTGGTGTT
XM_005248264.2:c.430-66_430-65insTGTTGGGTGTGTTTGGTGTT XP_005248321.1:n.430-66_430-65insTGTTGGGTGTGTTTGGTGTT
XM_005248264.4:c.430-66_430-65insTGTTGGGTGTGTTTGGTGTT XP_005248321.1:n.430-66_430-65insTGTTGGGTGTGTTTGGTGTT
NM_004465.2:c.430-66_430-65insTGTTGGGTGTGTTTGGTGTT MANE Select NP_004456.1:n.430-66_430-65insTGTTGGGTGTGTTTGGTGTT