Canonical Allele Identifier: CA2695207644
Gene: GLI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41967821dup , CM000669.2:g.41967821dup GRCh38
NC_000007.13:g.42007419dup , CM000669.1:g.42007419dup GRCh37
NC_000007.12:g.41973944dup NCBI36
NG_008434.1:g.274201dup

Transcript Alleles

HGVS Amino-acid change
ENST00000395925.8:c.2207dup MANE Select ENSP00000379258.3:p.Ser737Ter
ENST00000677288.1:c.2033dup ENSP00000503986.1:p.Ser679Ter
ENST00000677605.1:c.2207dup ENSP00000503743.1:p.Ser737Ter
ENST00000678429.1:c.2207dup ENSP00000502957.1:p.Ser737Ter
ENST00000395925.7:c.2207dup ENSP00000379258.3:p.Ser737Ter
ENST00000479210.1:n.2184dup
NM_000168.5:c.2207dup NP_000159.3:p.Ser737Ter
XM_005249703.1:c.2207dup XP_005249760.1:p.Ser737Ter
XM_005249704.2:c.2207dup XP_005249761.1:p.Ser737Ter
XM_011515272.1:c.2207dup XP_011513574.1:p.Ser737Ter
XM_011515273.1:c.2207dup XP_011513575.1:p.Ser737Ter
XM_011515274.1:c.2030dup XP_011513576.1:p.Ser678Ter
XM_011515274.2:c.2030dup XP_011513576.1:p.Ser678Ter
XM_017011997.1:c.2204dup XP_016867486.1:p.Ser736Ter
NM_000168.6:c.2207dup MANE Select NP_000159.3:p.Ser737Ter