Canonical Allele Identifier: CA343641250

Gene: GLUL

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.182386404T>C , CM000663.2:g.182386404T>C	GRCh38
NC_000001.10:g.182355539T>C , CM000663.1:g.182355539T>C	GRCh37
NC_000001.9:g.180622162T>C	NCBI36
NG_013347.2:g.10803A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331872.11:c.329-2A>G MANE Select	ENSP00000356537.6:n.329-2A>G
ENST00000642379.1:c.731-2A>G	ENSP00000494022.1:n.731-2A>G
ENST00000311223.9:c.329-2A>G	ENSP00000307900.5:n.329-2A>G
ENST00000331872.10:c.329-2A>G	ENSP00000356537.5:n.329-2A>G
ENST00000339526.8:c.329-2A>G	ENSP00000344958.4:n.329-2A>G
ENST00000417584.6:c.329-2A>G	ENSP00000398320.2:n.329-2A>G
ENST00000463851.6:n.129-562A>G
ENST00000475808.5:n.661-2A>G
ENST00000480604.5:n.779-2A>G
ENST00000484996.5:n.941-2A>G
ENST00000489818.5:n.454-2A>G
ENST00000491322.1:n.2622A>G
ENST00000621524.1:c.329-2A>G	ENSP00000481855.1:n.329-2A>G
NM_001033044.3:c.329-2A>G	NP_001028216.1:n.329-2A>G
NM_001033056.3:c.329-2A>G	NP_001028228.1:n.329-2A>G
NM_002065.6:c.329-2A>G	NP_002056.2:n.329-2A>G
XM_006711278.1:c.329-2A>G	XP_006711341.1:n.329-2A>G
XM_006711278.2:c.329-2A>G	XP_006711341.1:n.329-2A>G
NM_001033044.4:c.329-2A>G MANE Select	NP_001028216.1:n.329-2A>G
NM_001033056.4:c.329-2A>G	NP_001028228.1:n.329-2A>G
NM_002065.7:c.329-2A>G	NP_002056.2:n.329-2A>G