Canonical Allele Identifier: CA1543090370
Gene: FGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388291_44388292delinsAT , CM000667.2:g.44388291_44388292delinsAT GRCh38
NC_000005.9:g.44388393_44388394delinsAT , CM000667.1:g.44388393_44388394delinsAT GRCh37
NC_000005.8:g.44424150_44424151delinsAT NCBI36
NG_011446.1:g.5391_5392delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+66_325+67delinsAT MANE Select ENSP00000264664.4:n.325+66_325+67delinsAT
ENST00000264664.4:c.325+66_325+67delinsAT ENSP00000264664.4:n.325+66_325+67delinsAT
NM_004465.1:c.325+66_325+67delinsAT NP_004456.1:n.325+66_325+67delinsAT
XM_005248264.2:c.325+66_325+67delinsAT XP_005248321.1:n.325+66_325+67delinsAT
XM_005248264.4:c.325+66_325+67delinsAT XP_005248321.1:n.325+66_325+67delinsAT
NM_004465.2:c.325+66_325+67delinsAT MANE Select NP_004456.1:n.325+66_325+67delinsAT