Canonical Allele Identifier: CA367319007

Gene: GLI3

Linked Data

• gnomAD v4: 7-41965897-T-G
• MyVariant Identifiers: chr7:g.42005495T>G (hg19) ; chr7:g.41965897T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41965897T>G , CM000669.2:g.41965897T>G	GRCh38
NC_000007.13:g.42005495T>G , CM000669.1:g.42005495T>G	GRCh37
NC_000007.12:g.41972020T>G	NCBI36
NG_008434.1:g.276124A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.3176A>C MANE Select	ENSP00000379258.3:p.Asn1059Thr
ENST00000677288.1:c.3002A>C	ENSP00000503986.1:p.Asn1001Thr
ENST00000677605.1:c.3176A>C	ENSP00000503743.1:p.Asn1059Thr
ENST00000678429.1:c.3176A>C	ENSP00000502957.1:p.Asn1059Thr
ENST00000395925.7:c.3176A>C	ENSP00000379258.3:p.Asn1059Thr
ENST00000479210.1:n.3153A>C
NM_000168.5:c.3176A>C	NP_000159.3:p.Asn1059Thr
XM_005249703.1:c.3176A>C	XP_005249760.1:p.Asn1059Thr
XM_005249704.2:c.3176A>C	XP_005249761.1:p.Asn1059Thr
XM_011515272.1:c.3176A>C	XP_011513574.1:p.Asn1059Thr
XM_011515273.1:c.3176A>C	XP_011513575.1:p.Asn1059Thr
XM_011515274.1:c.2999A>C	XP_011513576.1:p.Asn1000Thr
XM_011515274.2:c.2999A>C	XP_011513576.1:p.Asn1000Thr
XM_017011997.1:c.3173A>C	XP_016867486.1:p.Asn1058Thr
NM_000168.6:c.3176A>C MANE Select	NP_000159.3:p.Asn1059Thr