Canonical Allele Identifier: CA2682510066
Gene: GLI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41965980dup , CM000669.2:g.41965980dup GRCh38
NC_000007.13:g.42005578dup , CM000669.1:g.42005578dup GRCh37
NC_000007.12:g.41972103dup NCBI36
NG_008434.1:g.276046dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000395925.8:c.3098dup MANE Select ENSP00000379258.3:p.Ala1034GlyfsTer?
ENST00000677288.1:c.2924dup ENSP00000503986.1:p.Ala976GlyfsTer?
ENST00000677605.1:c.3098dup ENSP00000503743.1:p.Ala1034GlyfsTer?
ENST00000678429.1:c.3098dup ENSP00000502957.1:p.Ala1034GlyfsTer?
ENST00000395925.7:c.3098dup ENSP00000379258.3:p.Ala1034GlyfsTer?
ENST00000479210.1:n.3075dup
NM_000168.5:c.3098dup NP_000159.3:p.Ala1034GlyfsTer?
XM_005249703.1:c.3098dup XP_005249760.1:p.Ala1034GlyfsTer?
XM_005249704.2:c.3098dup XP_005249761.1:p.Ala1034GlyfsTer?
XM_011515272.1:c.3098dup XP_011513574.1:p.Ala1034GlyfsTer?
XM_011515273.1:c.3098dup XP_011513575.1:p.Ala1034GlyfsTer?
XM_011515274.1:c.2921dup XP_011513576.1:p.Ala975GlyfsTer?
XM_011515274.2:c.2921dup XP_011513576.1:p.Ala975GlyfsTer?
XM_017011997.1:c.3095dup XP_016867486.1:p.Ala1033GlyfsTer?
NM_000168.6:c.3098dup MANE Select NP_000159.3:p.Ala1034GlyfsTer?