Canonical Allele Identifier: CA454661930

Gene: GLI3

Linked Data

• gnomAD v4: 7-41965596-G-T
• MyVariant Identifiers: chr7:g.42005194G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41965596G>T , CM000669.2:g.41965596G>T	GRCh38
NC_000007.13:g.42005194G>T , CM000669.1:g.42005194G>T	GRCh37
NC_000007.12:g.41971719G>T	NCBI36
NG_008434.1:g.276425C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.3477C>A MANE Select	ENSP00000379258.3:p.Pro1159=
ENST00000677288.1:c.3303C>A	ENSP00000503986.1:p.Pro1101=
ENST00000677605.1:c.3477C>A	ENSP00000503743.1:p.Pro1159=
ENST00000678429.1:c.3477C>A	ENSP00000502957.1:p.Pro1159=
ENST00000395925.7:c.3477C>A	ENSP00000379258.3:p.Pro1159=
ENST00000479210.1:n.3454C>A
NM_000168.5:c.3477C>A	NP_000159.3:p.Pro1159=
XM_005249703.1:c.3477C>A	XP_005249760.1:p.Pro1159=
XM_005249704.2:c.3477C>A	XP_005249761.1:p.Pro1159=
XM_011515272.1:c.3477C>A	XP_011513574.1:p.Pro1159=
XM_011515273.1:c.3477C>A	XP_011513575.1:p.Pro1159=
XM_011515274.1:c.3300C>A	XP_011513576.1:p.Pro1100=
XM_011515274.2:c.3300C>A	XP_011513576.1:p.Pro1100=
XM_017011997.1:c.3474C>A	XP_016867486.1:p.Pro1158=
NM_000168.6:c.3477C>A MANE Select	NP_000159.3:p.Pro1159=