Canonical Allele Identifier: CA454525793

Gene: GLI3

Linked Data

• gnomAD v4: 7-41972526-G-A
• MyVariant Identifiers: chr7:g.42012125G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41972526G>A , CM000669.2:g.41972526G>A	GRCh38
NC_000007.13:g.42012125G>A , CM000669.1:g.42012125G>A	GRCh37
NC_000007.12:g.41978650G>A	NCBI36
NG_008434.1:g.269494C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.1914C>T MANE Select	ENSP00000379258.3:p.Val638=
ENST00000677288.1:c.1740C>T	ENSP00000503986.1:p.Val580=
ENST00000677605.1:c.1914C>T	ENSP00000503743.1:p.Val638=
ENST00000678429.1:c.1914C>T	ENSP00000502957.1:p.Val638=
ENST00000395925.7:c.1914C>T	ENSP00000379258.3:p.Val638=
ENST00000464291.1:n.467C>T
ENST00000479210.1:n.1891C>T
NM_000168.5:c.1914C>T	NP_000159.3:p.Val638=
XM_005249703.1:c.1914C>T	XP_005249760.1:p.Val638=
XM_005249704.2:c.1914C>T	XP_005249761.1:p.Val638=
XM_011515272.1:c.1914C>T	XP_011513574.1:p.Val638=
XM_011515273.1:c.1914C>T	XP_011513575.1:p.Val638=
XM_011515274.1:c.1737C>T	XP_011513576.1:p.Val579=
XM_011515274.2:c.1737C>T	XP_011513576.1:p.Val579=
XM_017011997.1:c.1911C>T	XP_016867486.1:p.Val637=
NM_000168.6:c.1914C>T MANE Select	NP_000159.3:p.Val638=