Canonical Allele Identifier: CA367333157

Gene: GLI3

Linked Data

• MyVariant Identifiers: chr7:g.42088176T>A (hg19) ; chr7:g.42048577T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42048577T>A , CM000669.2:g.42048577T>A	GRCh38
NC_000007.13:g.42088176T>A , CM000669.1:g.42088176T>A	GRCh37
NC_000007.12:g.42054701T>A	NCBI36
NG_008434.1:g.193443A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.593A>T MANE Select	ENSP00000379258.3:p.Asn198Ile
ENST00000677288.1:c.416A>T	ENSP00000503986.1:p.Asn139Ile
ENST00000677605.1:c.593A>T	ENSP00000503743.1:p.Asn198Ile
ENST00000678429.1:c.593A>T	ENSP00000502957.1:p.Asn198Ile
ENST00000395925.7:c.593A>T	ENSP00000379258.3:p.Asn198Ile
ENST00000479210.1:n.570A>T
NM_000168.5:c.593A>T	NP_000159.3:p.Asn198Ile
XM_005249703.1:c.593A>T	XP_005249760.1:p.Asn198Ile
XM_005249704.2:c.593A>T	XP_005249761.1:p.Asn198Ile
XM_011515272.1:c.593A>T	XP_011513574.1:p.Asn198Ile
XM_011515273.1:c.593A>T	XP_011513575.1:p.Asn198Ile
XM_011515274.1:c.416A>T	XP_011513576.1:p.Asn139Ile
XM_011515274.2:c.416A>T	XP_011513576.1:p.Asn139Ile
XM_017011997.1:c.590A>T	XP_016867486.1:p.Asn197Ile
NM_000168.6:c.593A>T MANE Select	NP_000159.3:p.Asn198Ile