Canonical Allele Identifier: CA2176825361

Gene: GLDN

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51360976C= , CM000677.2:g.51360976C=	GRCh38
NC_000015.9:g.51653173C= , CM000677.1:g.51653173C=	GRCh37
NC_000015.8:g.49440465C=	NCBI36
NG_054933.1:g.24461C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000335449.11:c.364-16473C= MANE Select	ENSP00000335196.6:n.364-16473C=
ENST00000335449.10:c.364-16473C=	ENSP00000335196.6:n.364-16473C=
ENST00000558286.5:n.174+18929C=
ENST00000559317.5:n.284+439C=
ENST00000560215.5:c.251-16473C=
ENST00000560690.5:n.141-16473C=
NM_181789.2:c.364-16473C=	NP_861454.2:n.364-16473C=
NM_181789.3:c.364-16473C=	NP_861454.2:n.364-16473C=
XM_017022121.1:c.364-16473C=	XP_016877610.1:n.364-16473C=
XM_017022122.2:c.-10+439C=	XP_016877611.1:n.-10+439C=
XM_017022124.2:c.-9-16473C=	XP_016877613.1:n.-9-16473C=
XM_017022125.1:c.364-16473C=	XP_016877614.1:n.364-16473C=
XM_017022126.2:c.-9-16473C=	XP_016877615.1:n.-9-16473C=
NM_181789.4:c.364-16473C= MANE Select	NP_861454.2:n.364-16473C=