Canonical Allele Identifier: CA156907414

Gene: GLI3

Linked Data

• dbSNP Id: rs929846188
• gnomAD v4: 7-42040126-G-C
• MyVariant Identifiers: chr7:g.42079725G>C (hg19) ; chr7:g.42040126G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42040126G>C , CM000669.2:g.42040126G>C	GRCh38
NC_000007.13:g.42079725G>C , CM000669.1:g.42079725G>C	GRCh37
NC_000007.12:g.42046250G>C	NCBI36
NG_008434.1:g.201894C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.940C>G MANE Select	ENSP00000379258.3:p.Pro314Ala
ENST00000677288.1:c.763C>G	ENSP00000503986.1:p.Pro255Ala
ENST00000677605.1:c.940C>G	ENSP00000503743.1:p.Pro314Ala
ENST00000678429.1:c.940C>G	ENSP00000502957.1:p.Pro314Ala
ENST00000395925.7:c.940C>G	ENSP00000379258.3:p.Pro314Ala
ENST00000479210.1:n.917C>G
NM_000168.5:c.940C>G	NP_000159.3:p.Pro314Ala
XM_005249703.1:c.940C>G	XP_005249760.1:p.Pro314Ala
XM_005249704.2:c.940C>G	XP_005249761.1:p.Pro314Ala
XM_011515272.1:c.940C>G	XP_011513574.1:p.Pro314Ala
XM_011515273.1:c.940C>G	XP_011513575.1:p.Pro314Ala
XM_011515274.1:c.763C>G	XP_011513576.1:p.Pro255Ala
XM_011515274.2:c.763C>G	XP_011513576.1:p.Pro255Ala
XM_017011997.1:c.937C>G	XP_016867486.1:p.Pro313Ala
NM_000168.6:c.940C>G MANE Select	NP_000159.3:p.Pro314Ala