Canonical Allele Identifier: CA367322502

Gene: GLI3

Linked Data

• gnomAD v4: 7-41972533-G-A
• MyVariant Identifiers: chr7:g.42012132G>A (hg19) ; chr7:g.41972533G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41972533G>A , CM000669.2:g.41972533G>A	GRCh38
NC_000007.13:g.42012132G>A , CM000669.1:g.42012132G>A	GRCh37
NC_000007.12:g.41978657G>A	NCBI36
NG_008434.1:g.269487C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.1907C>T MANE Select	ENSP00000379258.3:p.Ala636Val
ENST00000677288.1:c.1733C>T	ENSP00000503986.1:p.Ala578Val
ENST00000677605.1:c.1907C>T	ENSP00000503743.1:p.Ala636Val
ENST00000678429.1:c.1907C>T	ENSP00000502957.1:p.Ala636Val
ENST00000395925.7:c.1907C>T	ENSP00000379258.3:p.Ala636Val
ENST00000464291.1:n.460C>T
ENST00000479210.1:n.1884C>T
NM_000168.5:c.1907C>T	NP_000159.3:p.Ala636Val
XM_005249703.1:c.1907C>T	XP_005249760.1:p.Ala636Val
XM_005249704.2:c.1907C>T	XP_005249761.1:p.Ala636Val
XM_011515272.1:c.1907C>T	XP_011513574.1:p.Ala636Val
XM_011515273.1:c.1907C>T	XP_011513575.1:p.Ala636Val
XM_011515274.1:c.1730C>T	XP_011513576.1:p.Ala577Val
XM_011515274.2:c.1730C>T	XP_011513576.1:p.Ala577Val
XM_017011997.1:c.1904C>T	XP_016867486.1:p.Ala635Val
NM_000168.6:c.1907C>T MANE Select	NP_000159.3:p.Ala636Val