Canonical Allele Identifier: CA342916
Gene: GLI3 HGNC NCBI

Linked Data

dbSNP Id: rs116840747

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41972378C>A , CM000669.2:g.41972378C>A GRCh38
NC_000007.13:g.42011977C>A , CM000669.1:g.42011977C>A GRCh37
NC_000007.12:g.41978502C>A NCBI36
NG_008434.1:g.269642G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000395925.8:c.2062G>T MANE Select ENSP00000379258.3:p.Glu688Ter
ENST00000677288.1:c.1888G>T ENSP00000503986.1:p.Glu630Ter
ENST00000677605.1:c.2062G>T ENSP00000503743.1:p.Glu688Ter
ENST00000678429.1:c.2062G>T ENSP00000502957.1:p.Glu688Ter
ENST00000395925.7:c.2062G>T ENSP00000379258.3:p.Glu688Ter
ENST00000479210.1:n.2039G>T
NM_000168.5:c.2062G>T NP_000159.3:p.Glu688Ter
XM_005249703.1:c.2062G>T XP_005249760.1:p.Glu688Ter
XM_005249704.2:c.2062G>T XP_005249761.1:p.Glu688Ter
XM_011515272.1:c.2062G>T XP_011513574.1:p.Glu688Ter
XM_011515273.1:c.2062G>T XP_011513575.1:p.Glu688Ter
XM_011515274.1:c.1885G>T XP_011513576.1:p.Glu629Ter
XM_011515274.2:c.1885G>T XP_011513576.1:p.Glu629Ter
XM_017011997.1:c.2059G>T XP_016867486.1:p.Glu687Ter
NM_000168.6:c.2062G>T MANE Select NP_000159.3:p.Glu688Ter