Canonical Allele Identifier: CA367322307
Gene: GLI3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41972489G>T , CM000669.2:g.41972489G>T GRCh38
NC_000007.13:g.42012088G>T , CM000669.1:g.42012088G>T GRCh37
NC_000007.12:g.41978613G>T NCBI36
NG_008434.1:g.269531C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395925.8:c.1951C>A MANE Select ENSP00000379258.3:p.Pro651Thr
ENST00000677288.1:c.1777C>A ENSP00000503986.1:p.Pro593Thr
ENST00000677605.1:c.1951C>A ENSP00000503743.1:p.Pro651Thr
ENST00000678429.1:c.1951C>A ENSP00000502957.1:p.Pro651Thr
ENST00000395925.7:c.1951C>A ENSP00000379258.3:p.Pro651Thr
ENST00000464291.1:n.504C>A
ENST00000479210.1:n.1928C>A
NM_000168.5:c.1951C>A NP_000159.3:p.Pro651Thr
XM_005249703.1:c.1951C>A XP_005249760.1:p.Pro651Thr
XM_005249704.2:c.1951C>A XP_005249761.1:p.Pro651Thr
XM_011515272.1:c.1951C>A XP_011513574.1:p.Pro651Thr
XM_011515273.1:c.1951C>A XP_011513575.1:p.Pro651Thr
XM_011515274.1:c.1774C>A XP_011513576.1:p.Pro592Thr
XM_011515274.2:c.1774C>A XP_011513576.1:p.Pro592Thr
XM_017011997.1:c.1948C>A XP_016867486.1:p.Pro650Thr
NM_000168.6:c.1951C>A MANE Select NP_000159.3:p.Pro651Thr