Canonical Allele Identifier: CA463832560
Gene: GLIS3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.3932465A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.3932465A>G , CM000671.2:g.3932465A>G GRCh38
NC_000009.11:g.3932465A>G , CM000671.1:g.3932465A>G GRCh37
NC_000009.10:g.3922465A>G NCBI36
NG_011782.1:g.372571T>C
NG_011782.2:g.372571T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463680.6:n.168T>C
ENST00000464391.2:n.436T>C
ENST00000491889.6:c.*1241T>C ENSP00000419914.1:n.*1241T>C
ENST00000645252.2:n.320T>C
ENST00000682749.1:c.1413T>C ENSP00000507306.1:p.Pro471=
ENST00000682846.1:c.132-102973T>C ENSP00000507527.1:n.132-102973T>C
ENST00000682864.1:n.397-20T>C
ENST00000381971.8:c.1878T>C MANE Select ENSP00000371398.3:p.Pro626=
ENST00000645252.1:n.320T>C
ENST00000324333.14:c.1413T>C ENSP00000325494.10:p.Pro471=
ENST00000381971.7:c.1878T>C ENSP00000371398.3:p.Pro626=
ENST00000461870.5:n.234T>C
ENST00000463680.5:n.168T>C
ENST00000464391.1:n.426T>C
ENST00000467497.6:n.418T>C
NM_001042413.1:c.1878T>C NP_001035878.1:p.Pro626=
NM_152629.3:c.1413T>C NP_689842.3:p.Pro471=
XM_005251386.3:c.1413T>C XP_005251443.1:p.Pro471=
XM_005251387.3:c.1212T>C XP_005251444.1:p.Pro404=
XM_005251388.3:c.1212T>C XP_005251445.1:p.Pro404=
XM_011517763.1:c.1878T>C XP_011516065.1:p.Pro626=
XM_011517764.1:c.1878T>C XP_011516066.1:p.Pro626=
XM_011517765.1:c.1878T>C XP_011516067.1:p.Pro626=
XM_011517766.1:c.1413T>C XP_011516068.1:p.Pro471=
XM_011517767.1:c.1212T>C XP_011516069.1:p.Pro404=
XM_005251386.4:c.1413T>C XP_005251443.1:p.Pro471=
XM_005251387.4:c.1212T>C XP_005251444.1:p.Pro404=
XM_005251388.4:c.1212T>C XP_005251445.1:p.Pro404=
XM_011517763.2:c.1878T>C XP_011516065.1:p.Pro626=
XM_011517764.2:c.1878T>C XP_011516066.1:p.Pro626=
XM_011517765.2:c.1878T>C XP_011516067.1:p.Pro626=
XM_011517766.2:c.1413T>C XP_011516068.1:p.Pro471=
XM_011517767.3:c.1212T>C XP_011516069.1:p.Pro404=
XM_017014361.1:c.1413T>C XP_016869850.1:p.Pro471=
NM_001042413.2:c.1878T>C MANE Select NP_001035878.1:p.Pro626=
NM_152629.4:c.1413T>C NP_689842.3:p.Pro471=