Canonical Allele Identifier: CA464495412

Gene: GNE CLTA

Linked Data

• ClinVar Variation Id: 1113015
• ClinVar RCV Id: RCV001440213
• dbSNP Id: rs2133024607
• gnomAD v4: 9-36223461-G-T
• COSMIC: COSM4626455 ; COSM4626456 ; COSM4626457
• MyVariant Identifiers: chr9:g.36223458G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36223461G>T , CM000671.2:g.36223461G>T	GRCh38
NC_000009.11:g.36223458G>T , CM000671.1:g.36223458G>T	GRCh37
NC_000009.10:g.36213458G>T	NCBI36
NG_008246.1:g.58584C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.1416C>A (GNE) MANE Plus Clinical	ENSP00000379839.3:p.Thr472=
ENST00000543356.7:c.1146C>A (GNE)	ENSP00000437765.3:p.Thr382=
ENST00000642385.2:c.1323C>A (GNE) MANE Select	ENSP00000494141.2:p.Thr441=
ENST00000377902.5:c.1323C>A (GNE)	ENSP00000367134.4:p.Thr441=
ENST00000396594.7:c.1416C>A (GNE)	ENSP00000379839.3:p.Thr472=
ENST00000447283.6:c.1323C>A (GNE)	ENSP00000414760.2:p.Thr441=
ENST00000464497.5:c.485+19282G>T (CLTA)	ENSP00000419158.1:n.485+19282G>T
ENST00000539208.5:c.993C>A (GNE)	ENSP00000445117.1:p.Thr331=
ENST00000539815.5:c.1323C>A (GNE)	ENSP00000439155.1:p.Thr441=
ENST00000543356.6:c.1308C>A (GNE)	ENSP00000437765.2:p.Thr436=
NM_001128227.2:c.1416C>A (GNE)	NP_001121699.1:p.Thr472=
NM_001190383.1:c.1323C>A (GNE)	NP_001177312.1:p.Thr441=
NM_001190384.1:c.993C>A (GNE)	NP_001177313.1:p.Thr331=
NM_001190388.1:c.1308C>A (GNE)	NP_001177317.1:p.Thr436=
NM_005476.5:c.1323C>A (GNE)	NP_005467.1:p.Thr441=
XM_005251334.3:c.1263C>A (GNE)	XP_005251391.1:p.Thr421=
NM_001190383.2:c.1323C>A (GNE)	NP_001177312.1:p.Thr441=
NM_001190384.2:c.993C>A (GNE)	NP_001177313.1:p.Thr331=
NM_005476.6:c.1323C>A (GNE)	NP_005467.1:p.Thr441=
XM_005251334.4:c.1263C>A (GNE)	XP_005251391.1:p.Thr421=
XM_017014167.1:c.1323C>A (GNE)	XP_016869656.1:p.Thr441=
XM_017014168.1:c.1170C>A (GNE)	XP_016869657.1:p.Thr390=
NM_001128227.3:c.1416C>A (GNE) MANE Plus Clinical	NP_001121699.1:p.Thr472=
NM_001190383.3:c.1323C>A (GNE)	NP_001177312.1:p.Thr441=
NM_001190384.3:c.993C>A (GNE)	NP_001177313.1:p.Thr331=
NM_001190388.2:c.1146C>A (GNE)	NP_001177317.2:p.Thr382=
NM_001374797.1:c.1170C>A (GNE)	NP_001361726.1:p.Thr390=
NM_001374798.1:c.1146C>A (GNE)	NP_001361727.1:p.Thr382=
NM_005476.7:c.1323C>A (GNE) MANE Select	NP_005467.1:p.Thr441=