Canonical Allele Identifier: CA394594295

Gene: GLIS2 PAM16

Linked Data

• MyVariant Identifiers: chr16:g.4383474C>G (hg19) ; chr16:g.4333473C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4333473C>G , CM000678.2:g.4333473C>G	GRCh38
NC_000016.9:g.4383474C>G , CM000678.1:g.4383474C>G	GRCh37
NC_000016.8:g.4323475C>G	NCBI36
NG_016391.1:g.6250C>G
NG_016391.2:g.23713C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433375.2:c.299C>G (GLIS2) MANE Select	ENSP00000395547.1:p.Pro100Arg
ENST00000262366.7:c.299C>G (GLIS2)	ENSP00000262366.3:p.Pro100Arg
ENST00000433375.1:c.299C>G (GLIS2)	ENSP00000395547.1:p.Pro100Arg
ENST00000577031.5:c.292-1699G>C (PAM16)	ENSP00000459113.1:n.292-1699G>C
NM_032575.2:c.299C>G (GLIS2)	NP_115964.2:p.Pro100Arg
XM_005255641.3:c.299C>G (GLIS2)	XP_005255698.1:p.Pro100Arg
XM_005255642.2:c.299C>G (GLIS2)	XP_005255699.1:p.Pro100Arg
NM_001318918.1:c.299C>G (GLIS2)	NP_001305847.1:p.Pro100Arg
XM_005255641.4:c.299C>G (GLIS2)	XP_005255698.1:p.Pro100Arg
NM_032575.3:c.299C>G (GLIS2) MANE Select	NP_115964.2:p.Pro100Arg
NM_001318918.2:c.299C>G (GLIS2)	NP_001305847.1:p.Pro100Arg