Canonical Allele Identifier: CA4230895

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42025331A>G , CM000669.2:g.42025331A>G	GRCh38
NC_000007.13:g.42064930A>G , CM000669.1:g.42064930A>G	GRCh37
NC_000007.12:g.42031455A>G	NCBI36
NG_008434.1:g.216689T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.1289T>C MANE Select	ENSP00000379258.3:p.Met430Thr
ENST00000677288.1:c.1115T>C	ENSP00000503986.1:p.Met372Thr
ENST00000677605.1:c.1289T>C	ENSP00000503743.1:p.Met430Thr
ENST00000678429.1:c.1289T>C	ENSP00000502957.1:p.Met430Thr
ENST00000395925.7:c.1289T>C	ENSP00000379258.3:p.Met430Thr
ENST00000479210.1:n.1266T>C
NM_000168.5:c.1289T>C	NP_000159.3:p.Met430Thr
XM_005249703.1:c.1289T>C	XP_005249760.1:p.Met430Thr
XM_005249704.2:c.1289T>C	XP_005249761.1:p.Met430Thr
XM_011515272.1:c.1289T>C	XP_011513574.1:p.Met430Thr
XM_011515273.1:c.1289T>C	XP_011513575.1:p.Met430Thr
XM_011515274.1:c.1112T>C	XP_011513576.1:p.Met371Thr
XM_011515274.2:c.1112T>C	XP_011513576.1:p.Met371Thr
XM_017011997.1:c.1286T>C	XP_016867486.1:p.Met429Thr
NM_000168.6:c.1289T>C MANE Select	NP_000159.3:p.Met430Thr