Canonical Allele Identifier: CA1702647580
Gene: GLI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41972307G= , CM000669.2:g.41972307G= GRCh38
NC_000007.13:g.42011906G= , CM000669.1:g.42011906G= GRCh37
NC_000007.12:g.41978431G= NCBI36
NG_008434.1:g.269713C=

Transcript Alleles

HGVS Amino-acid change
ENST00000395925.8:c.2103+30C= MANE Select ENSP00000379258.3:n.2103+30C=
ENST00000677288.1:c.1929+30C= ENSP00000503986.1:n.1929+30C=
ENST00000677605.1:c.2103+30C= ENSP00000503743.1:n.2103+30C=
ENST00000678429.1:c.2103+30C= ENSP00000502957.1:n.2103+30C=
ENST00000395925.7:c.2103+30C= ENSP00000379258.3:n.2103+30C=
ENST00000479210.1:n.2080+30C=
NM_000168.5:c.2103+30C= NP_000159.3:n.2103+30C=
XM_005249703.1:c.2103+30C= XP_005249760.1:n.2103+30C=
XM_005249704.2:c.2103+30C= XP_005249761.1:n.2103+30C=
XM_011515272.1:c.2103+30C= XP_011513574.1:n.2103+30C=
XM_011515273.1:c.2103+30C= XP_011513575.1:n.2103+30C=
XM_011515274.1:c.1926+30C= XP_011513576.1:n.1926+30C=
XM_011515274.2:c.1926+30C= XP_011513576.1:n.1926+30C=
XM_017011997.1:c.2100+30C= XP_016867486.1:n.2100+30C=
NM_000168.6:c.2103+30C= MANE Select NP_000159.3:n.2103+30C=