Canonical Allele Identifier: CA394594192

Gene: GLIS2 PAM16

Linked Data

• MyVariant Identifiers: chr16:g.4383420G>C (hg19) ; chr16:g.4333419G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4333419G>C , CM000678.2:g.4333419G>C	GRCh38
NC_000016.9:g.4383420G>C , CM000678.1:g.4383420G>C	GRCh37
NC_000016.8:g.4323421G>C	NCBI36
NG_016391.1:g.6196G>C
NG_016391.2:g.23659G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433375.2:c.245G>C (GLIS2) MANE Select	ENSP00000395547.1:p.Ser82Thr
ENST00000262366.7:c.245G>C (GLIS2)	ENSP00000262366.3:p.Ser82Thr
ENST00000433375.1:c.245G>C (GLIS2)	ENSP00000395547.1:p.Ser82Thr
ENST00000577031.5:c.292-1645C>G (PAM16)	ENSP00000459113.1:n.292-1645C>G
NM_032575.2:c.245G>C (GLIS2)	NP_115964.2:p.Ser82Thr
XM_005255641.3:c.245G>C (GLIS2)	XP_005255698.1:p.Ser82Thr
XM_005255642.2:c.245G>C (GLIS2)	XP_005255699.1:p.Ser82Thr
NM_001318918.1:c.245G>C (GLIS2)	NP_001305847.1:p.Ser82Thr
XM_005255641.4:c.245G>C (GLIS2)	XP_005255698.1:p.Ser82Thr
NM_032575.3:c.245G>C (GLIS2) MANE Select	NP_115964.2:p.Ser82Thr
NM_001318918.2:c.245G>C (GLIS2)	NP_001305847.1:p.Ser82Thr