Canonical Allele Identifier: CA1828993248

Gene: GLIS3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.3932477_3932481delinsGAGAA , CM000671.2:g.3932477_3932481delinsGAGAA	GRCh38
NC_000009.11:g.3932477_3932481delinsGAGAA , CM000671.1:g.3932477_3932481delinsGAGAA	GRCh37
NC_000009.10:g.3922477_3922481delinsGAGAA	NCBI36
NG_011782.1:g.372555_372559delinsTTCTC
NG_011782.2:g.372555_372559delinsTTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463680.6:n.163-11_163-7delinsTTCTC
ENST00000464391.2:n.431-11_431-7delinsTTCTC
ENST00000491889.6:c.*1236-11_*1236-7delinsTTCTC	ENSP00000419914.1:n.*1236-11_*1236-7delinsTTCTC
ENST00000645252.2:n.315-11_315-7delinsTTCTC
ENST00000682749.1:c.1408-11_1408-7delinsTTCTC	ENSP00000507306.1:n.1408-11_1408-7delinsTTCTC
ENST00000682846.1:c.132-102989_132-102985delinsTTCTC	ENSP00000507527.1:n.132-102989_132-102985delinsTTCTC
ENST00000682864.1:n.397-36_397-32delinsTTCTC
ENST00000381971.8:c.1873-11_1873-7delinsTTCTC MANE Select	ENSP00000371398.3:n.1873-11_1873-7delinsTTCTC
ENST00000645252.1:n.315-11_315-7delinsTTCTC
ENST00000324333.14:c.1408-11_1408-7delinsTTCTC	ENSP00000325494.10:n.1408-11_1408-7delinsTTCTC
ENST00000381971.7:c.1873-11_1873-7delinsTTCTC	ENSP00000371398.3:n.1873-11_1873-7delinsTTCTC
ENST00000461870.5:n.229-11_229-7delinsTTCTC
ENST00000463680.5:n.163-11_163-7delinsTTCTC
ENST00000464391.1:n.421-11_421-7delinsTTCTC
ENST00000467497.6:n.413-11_413-7delinsTTCTC
NM_001042413.1:c.1873-11_1873-7delinsTTCTC	NP_001035878.1:n.1873-11_1873-7delinsTTCTC
NM_152629.3:c.1408-11_1408-7delinsTTCTC	NP_689842.3:n.1408-11_1408-7delinsTTCTC
XM_005251386.3:c.1408-11_1408-7delinsTTCTC	XP_005251443.1:n.1408-11_1408-7delinsTTCTC
XM_005251387.3:c.1207-11_1207-7delinsTTCTC	XP_005251444.1:n.1207-11_1207-7delinsTTCTC
XM_005251388.3:c.1207-11_1207-7delinsTTCTC	XP_005251445.1:n.1207-11_1207-7delinsTTCTC
XM_011517763.1:c.1873-11_1873-7delinsTTCTC	XP_011516065.1:n.1873-11_1873-7delinsTTCTC
XM_011517764.1:c.1873-11_1873-7delinsTTCTC	XP_011516066.1:n.1873-11_1873-7delinsTTCTC
XM_011517765.1:c.1873-11_1873-7delinsTTCTC	XP_011516067.1:n.1873-11_1873-7delinsTTCTC
XM_011517766.1:c.1408-11_1408-7delinsTTCTC	XP_011516068.1:n.1408-11_1408-7delinsTTCTC
XM_011517767.1:c.1207-11_1207-7delinsTTCTC	XP_011516069.1:n.1207-11_1207-7delinsTTCTC
XM_005251386.4:c.1408-11_1408-7delinsTTCTC	XP_005251443.1:n.1408-11_1408-7delinsTTCTC
XM_005251387.4:c.1207-11_1207-7delinsTTCTC	XP_005251444.1:n.1207-11_1207-7delinsTTCTC
XM_005251388.4:c.1207-11_1207-7delinsTTCTC	XP_005251445.1:n.1207-11_1207-7delinsTTCTC
XM_011517763.2:c.1873-11_1873-7delinsTTCTC	XP_011516065.1:n.1873-11_1873-7delinsTTCTC
XM_011517764.2:c.1873-11_1873-7delinsTTCTC	XP_011516066.1:n.1873-11_1873-7delinsTTCTC
XM_011517765.2:c.1873-11_1873-7delinsTTCTC	XP_011516067.1:n.1873-11_1873-7delinsTTCTC
XM_011517766.2:c.1408-11_1408-7delinsTTCTC	XP_011516068.1:n.1408-11_1408-7delinsTTCTC
XM_011517767.3:c.1207-11_1207-7delinsTTCTC	XP_011516069.1:n.1207-11_1207-7delinsTTCTC
XM_017014361.1:c.1408-11_1408-7delinsTTCTC	XP_016869850.1:n.1408-11_1408-7delinsTTCTC
NM_001042413.2:c.1873-11_1873-7delinsTTCTC MANE Select	NP_001035878.1:n.1873-11_1873-7delinsTTCTC
NM_152629.4:c.1408-11_1408-7delinsTTCTC	NP_689842.3:n.1408-11_1408-7delinsTTCTC