Canonical Allele Identifier: CA367329481

Gene: GLI3

Linked Data

• gnomAD v4: 7-42040102-T-A
• MyVariant Identifiers: chr7:g.42079701T>A (hg19) ; chr7:g.42040102T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42040102T>A , CM000669.2:g.42040102T>A	GRCh38
NC_000007.13:g.42079701T>A , CM000669.1:g.42079701T>A	GRCh37
NC_000007.12:g.42046226T>A	NCBI36
NG_008434.1:g.201918A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.964A>T MANE Select	ENSP00000379258.3:p.Asn322Tyr
ENST00000677288.1:c.787A>T	ENSP00000503986.1:p.Asn263Tyr
ENST00000677605.1:c.964A>T	ENSP00000503743.1:p.Asn322Tyr
ENST00000678429.1:c.964A>T	ENSP00000502957.1:p.Asn322Tyr
ENST00000395925.7:c.964A>T	ENSP00000379258.3:p.Asn322Tyr
ENST00000479210.1:n.941A>T
NM_000168.5:c.964A>T	NP_000159.3:p.Asn322Tyr
XM_005249703.1:c.964A>T	XP_005249760.1:p.Asn322Tyr
XM_005249704.2:c.964A>T	XP_005249761.1:p.Asn322Tyr
XM_011515272.1:c.964A>T	XP_011513574.1:p.Asn322Tyr
XM_011515273.1:c.964A>T	XP_011513575.1:p.Asn322Tyr
XM_011515274.1:c.787A>T	XP_011513576.1:p.Asn263Tyr
XM_011515274.2:c.787A>T	XP_011513576.1:p.Asn263Tyr
XM_017011997.1:c.961A>T	XP_016867486.1:p.Asn321Tyr
NM_000168.6:c.964A>T MANE Select	NP_000159.3:p.Asn322Tyr