Canonical Allele Identifier: CA1702754164
Gene: GLI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.42190309T= , CM000669.2:g.42190309T= GRCh38
NC_000007.13:g.42229908T= , CM000669.1:g.42229908T= GRCh37
NC_000007.12:g.42196433T= NCBI36
NG_008434.1:g.51711A=

Transcript Alleles

HGVS Amino-acid change
ENST00000395925.8:c.124+32821A= MANE Select ENSP00000379258.3:n.124+32821A=
ENST00000677605.1:c.124+32821A= ENSP00000503743.1:n.124+32821A=
ENST00000678429.1:c.124+32821A= ENSP00000502957.1:n.124+32821A=
ENST00000395925.7:c.124+32821A= ENSP00000379258.3:n.124+32821A=
ENST00000437480.1:c.125-17623A= ENSP00000407963.1:n.125-17623A=
ENST00000448703.5:c.124+32821A= ENSP00000406135.1:n.124+32821A=
NM_000168.5:c.124+32821A= NP_000159.3:n.124+32821A=
XM_005249703.1:c.124+32821A= XP_005249760.1:n.124+32821A=
XM_005249704.2:c.124+32821A= XP_005249761.1:n.124+32821A=
XM_011515272.1:c.124+32821A= XP_011513574.1:n.124+32821A=
XM_011515273.1:c.124+32821A= XP_011513575.1:n.124+32821A=
NM_000168.6:c.124+32821A= MANE Select NP_000159.3:n.124+32821A=