Canonical Allele Identifier: CA367322285

Gene: GLI3

Linked Data

• ClinVar Variation Id: 912075
• ClinVar RCV Id: RCV001165055 ; RCV001165054
• dbSNP Id: rs1787391168
• COSMIC: COSM4798483
• MyVariant Identifiers: chr7:g.42012082G>A (hg19) ; chr7:g.41972483G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41972483G>A , CM000669.2:g.41972483G>A	GRCh38
NC_000007.13:g.42012082G>A , CM000669.1:g.42012082G>A	GRCh37
NC_000007.12:g.41978607G>A	NCBI36
NG_008434.1:g.269537C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.1957C>T MANE Select	ENSP00000379258.3:p.Pro653Ser
ENST00000677288.1:c.1783C>T	ENSP00000503986.1:p.Pro595Ser
ENST00000677605.1:c.1957C>T	ENSP00000503743.1:p.Pro653Ser
ENST00000678429.1:c.1957C>T	ENSP00000502957.1:p.Pro653Ser
ENST00000395925.7:c.1957C>T	ENSP00000379258.3:p.Pro653Ser
ENST00000464291.1:n.510C>T
ENST00000479210.1:n.1934C>T
NM_000168.5:c.1957C>T	NP_000159.3:p.Pro653Ser
XM_005249703.1:c.1957C>T	XP_005249760.1:p.Pro653Ser
XM_005249704.2:c.1957C>T	XP_005249761.1:p.Pro653Ser
XM_011515272.1:c.1957C>T	XP_011513574.1:p.Pro653Ser
XM_011515273.1:c.1957C>T	XP_011513575.1:p.Pro653Ser
XM_011515274.1:c.1780C>T	XP_011513576.1:p.Pro594Ser
XM_011515274.2:c.1780C>T	XP_011513576.1:p.Pro594Ser
XM_017011997.1:c.1954C>T	XP_016867486.1:p.Pro652Ser
NM_000168.6:c.1957C>T MANE Select	NP_000159.3:p.Pro653Ser